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(en)Novel substituted formamidines are useful as ultraviolet light absorbers, the formamidines being characterized by the formula: ##STR1## wherein: R 1 represents an alkyl group containing one to five carbon atoms;
B is selected from the group consisting of H, OH, Cl or alkoxy;
R 2 represents a phenyl group or an alkyl group containing one to nine carbon atoms;
A is selected from the group consisting of H, carboalkoxy, alkoxy, alkyl, dimethylamino and halogen.
D is selected from the group consisting of H, methoxy and chlorine.
B is selected from the group consisting of H, OH, Cl or alkoxy;
R 2 represents a phenyl group or an alkyl group containing one to nine carbon atoms;
A is selected from the group consisting of H, carboalkoxy, alkoxy, alkyl, dimethylamino and halogen.
D is selected from the group consisting of H, methoxy and chlorine.
1.ApplicationNumber: US-46205174-A
1.PublishNumber: US-4021471-A
2.Date Publish: 19770503
3.Inventor: VIRGILIO; JOSEPH A.
MANOWITZ; MILTON
4.Inventor Harmonized: VIRGILIO JOSEPH A()
MANOWITZ MILTON()
5.Country: US
6.Claims:
(en)Novel substituted formamidines are useful as ultraviolet light absorbers, the formamidines being characterized by the formula: ##STR1## wherein: R 1 represents an alkyl group containing one to five carbon atoms;
B is selected from the group consisting of H, OH, Cl or alkoxy;
R 2 represents a phenyl group or an alkyl group containing one to nine carbon atoms;
A is selected from the group consisting of H, carboalkoxy, alkoxy, alkyl, dimethylamino and halogen.
D is selected from the group consisting of H, methoxy and chlorine.
7.Description:
(en)BACKGROUND OF THE INVENTION
1. Field of the Invention
This invention relates to novel formamidines useful for protecting materials against the degradative effects of ultraviolet light.
2. The Prior Art
It is known in the art that organic materials which possess ultraviolet light absorbing properties can be added to many other organic materials to protect these materials from being degraded or damaged by ultraviolet light. For example, various polymers, plastics, resins, cosmetics, dyes, pigments, lacquors, varnishes, textiles, etc. are subject to photodegradation by sunlight or ultraviolet radiation and such materials can often be protected by treatment with chemicals which will absorb the harmful rays and convert them to relatively harmless forms of energy.
The prior art does not teach that the novel substituted formamidines of this invention possess the outstanding light absorbing properties combined with the high photostability and thermal stability as herein disclosed.
SUMMARY OF THE INVENTION
In accordance with the present invention there is provided substituted formamidines of the general structure: ##STR2## wherein: R 1 represents an alkyl group containing one to five carbon atoms:
B is selected from the group consisting of H, OH, Cl or alkoxy;
R 2 represents a phenyl group or an alkyl group containing one to nine carbon atoms;
A is selected from the group consisting of H, carboalkoxy, alkoxy, alkyl, dimethylamino and halogen.
D is selected from the group consisting of H, methoxy and chlorine.
The formamidines of this invention are particularly valuable as U.V. screening agents. As will be demonstrated they absorb over a wide range of the U.V. spectrum being particularly effective in the range from 280-370 nanometers. The formanidines are colorless and soluble in most organic solvents.
More significant and surprising is their remarkable resistance to photodegradation and thermal degradation. The formamidines of this invention are from about 5 to 30 times more resistant to photodegradation than the commercially available 2-hydroxy-4-methoxybenzophenone. The thermal stability is also illustrated by the fact that most of the formamidines were distilled at temperatures (boiling point) above 200° C. Toward the end of such distillations temperatures in the distilling vessel exceeded 300° C. without any decomposition being noted. This resistance to thermal degradation is particularly useful in applications where high temperatures are required as, for example, in the molding of plastics.
The substituted formamidines of the present invention are prepared in a number of ways, the method chosen being dependent upon the starting material available.
A preferred method utilizes as intermediates the novel formimidates of the general formula: ##STR3## wherein: R 1 and B are as defined previously and R 3 is an alkyl group of from one to five carbons. The novel formamidates, II, are prepared by reacting the corresponding 4-aminobenzoate with a trialkyl orthoformate as illustrated below. The reaction is effected by heating the reactants from ##STR4## 80° C. to 200° C. and the preferred temperature range is 130° to 160° C. The preferred procedure is to remove the alcohol which is formed during the reaction. The reaction is stopped when no more alcohol is produced. Any trialkylorthoformate may be used but it is preferred to use the commercially available triethyl or trimethyl orthoformates.
The novel formamidines, I, can be prepared by reacting the novel formimidates, II, with N-alkylanalines of general structure IV, as illustrated below: I, II, A, D, R 2 and R 3 being as previously defined. Reaction is effected by heating the reactants ##STR5## from 80° C. to 250° C., the preferred temperature range being 170° C. to 210° C. A preferred procedure is to remove the alcohol which is formed during the reaction. The reaction is stopped when no more alcohol is produced.
The N-alkylanilines, IV, can be prepared by any of the general methods known in the art. The N-alkylanilines, IV, used in this invention were prepared from the corresponding anilines, V, as shown below: ##STR6##
Any of the methods known in the art for monoacylating primary amines, alkylating amides and hydrolysing amides can be used in the preparation of the desired N-alkylanilines, IV.
Another method for preparing the novel formamidines of this invention involves the reaction of an aminobenzoate of formula III with a formamide of the general formula VI in the presence of a suitable catalyst such as phosphorous pentachloride to form the formamidines of structure I as shown below: ##STR7##
Another method for preparing the novel formamidines of this invention involves the alkylation of formamidines of general formula VII by methods known in the art. ##STR8##
Detailed procedures of each of these methods are provided herein.
The strong ultraviolet light absorbing properties of the formamidines of this invention are demonstrated by dissolving the compounds in isopropanol and determining their spectrum using a recording ultraviolet spectrophotometer. Table I lists the wavelength of maximum absorption (λ max ), the intensity of this absorption calculated as molar extinction coefficient (ε), and the λ range where ε = 5,000 or greater.
TABLE I__________________________________________________________________________ λ range (nm)Compound Name .sup.λmax (nm) ε ε >5,000__________________________________________________________________________C.sub.1 N'-(4-Ethoxycarbonylphenyl)-N-methyl- 313 26,200 280 - 350* N-phenylformamidineC.sub.2 N'-(4-Ethoxycarbonylphenyl)-N-(4-methoxyphenyl)- 312 26,300 280 - 355 N-methylformamidineC.sub.3 N,N'-Bis(4-Ethoxycarbonylphenyl)-N-methyl- 323 32,800 280 - 365 formamidineC.sub.4 N-(4-Dimethylaminophenyl)-N'-(4-ethoxy- 324 22,100 280 - 368 carbonylphenyl)-N-methylformamidineC.sub.5 N'-(4-Ethoxycarbonylphenyl)-N-(2-methoxy- 312 27,500 280 - 357 phenyl)-N-methylformamidineC.sub.6 N'-(4-Ethoxycarbonylphenyl)-N-(3,4- 312 29,500 280 - 357 dichlorophenyl)-N-methylformamidineC.sub.7 N-(4-Butoxycarbonylphenyl)-N'-(4-ethoxy- 323 36,800 280 - 368 carbonylphenyl)-N-methylformamidineC.sub.8 N'-(4-Butoxycarbonylphenyl)-N-methyl- 312 27,100 280 - 355 N-phenylformamidineC.sub.9 N'-(3-Hydroxy-4-methoxycarbonylphenyl)- 320 26,814 280 - 357 N-methyl-N-phenylformamidineC.sub.10 N-Butyl-N-phenyl-N'-(4-ethoxycarbonyl- 312 26,700 280 - 362 phenyl)formamidineC.sub.11 N'-(4-Ethoxycarbonylphenyl)-N-(n-octyl)- 314 28,300 280 - 357 N-phenylformamidineC.sub.12 N,N-Diphenyl-N'-(4-ethoxycarbonylphenyl)- 317 25,300 280 - 357 formamidineC.sub.13 N'-(4-Ethoxycarbonyl-3-methoxyphenyl)- 320 27,000 280 - 358 N'-methyl-N-phenylformamidineC.sub.14 N'-(4-Isopropoxycarbonylphenyl)-N- 312 26,800 280 - 356 methyl-N-phenylformamidineC.sub.15 N'-(4-Ethoxycarbonylphenyl)-N-methyl-N-(p- 313 27,000 280 - 357 ethylphenylformamidineC.sub.16 N'-(2-Chloro-4-methoxycarbonylphenyl)-N- 318 25,800 280 - 360 methyl-N-phenylformamidine__________________________________________________________________________ *Only wavelengths above 280 nm were included.
The photostability of the formamidines of this invention was demonstrated in accelerated irradiation tests by exposing isopropanol solution of the compounds in pyrex flasks under a Hanovid lamp 679A (450 watts). Aliquots of these solutions were periodically examined spectrophotometrically to determine their rate of photodegradation. Results of these tests are listed in Table II including the test data for a commercially used hydroxybenzophenone type screening agent.
TABLE II______________________________________ Percent Degradation Exposure Time (hours)Compound O 8 16 24______________________________________C.sub.1 0 7 7 7C.sub.2 0 6 9 9C.sub.3 0 0 2 3C.sub.4 0 4 8 22C.sub.5 0 3 5 19C.sub.6 0 1 8 16C.sub.7 0 2 3 9C.sub.8 0 1 1 9C.sub.9 0 3 5 10C.sub.10 0 5 7 13C.sub.11 0 2 7 15C.sub.12 0 2 5 16 2-Hydroxy- 4-methoxy- benzophe- none 0 2 75 100______________________________________
The ability of the novel formamidines of this mixture to retard the discoloration of plastic films when incorporated therein is shown by the following described test and results.
Plastic films containing 0.4% by weight of the novel formamidines of this invention were prepared from a non-plasticized polyvinylchloride (87%) polyvinylacetate (13%) resin. The films were exposed to a Hanovia lamp 679A (450 watts) and periodically examined for discoloration. Results of these tests are listed in Table III using the following commercial ratings: o-no discoloration, 1-trace, 2-slight, 3-moderate, 4-severe.
TABLE III______________________________________ Discoloration Exposure Period (hours)Compound 0 8 16 24 48 80______________________________________Control 0 2 3 3 4 4C.sub.1 0 0 0 1 2 2C.sub.2 0 1 1 1 2 2C.sub.3 0 1 1 2 3 3C.sub.5 0 0 1 1 2 2C.sub.7 0 0 1 1 2 2C.sub.8 0 0 0 0 1 2C.sub.9 0 0 0 0 1 2______________________________________
The ability of the novel compound of this invention to retard the fading of dyes when incorporated therein is shown by the following described test and results.
Isopropanol solutions of the blue dye FD&C Blue No. 1, (H. Kohnstamm & Co.) containing 0.01% of a UV Absorber Formamidine of the invention were exposed to UV irradiation from G.E. fluorescent lamps F40BL. These solutions were periodically examined spectrophotometrically to determine the degree to which the dye has faded. The results are given in Table IV.
TABLE IV______________________________________FD&C Blue No. 1 Percent Degradation ofUV Absorber Versus Exposure Time (days)______________________________________ 14 20Control 100Tinuvin P 60 80C.sub.2 7 7C.sub.5 20 20C.sub.7 7 7C.sub.9 60 67______________________________________
The following examples are presented to provide a more detailed explanation of the present invention and are intended as illustrations and not limitations of the invention. Unless otherwise stated herein, the temperatures are in degrees Centigrade and all parts are by weight.
EXAMPLE I
Preparation of N'-(4-Ethoxycarbonylphenyl)-N-methyl-N-phenylformamidine
a. Ethyl (4-ethoxycarbonylphenyl)formimidate (a)
Ethyl 4-aminobenzoate (82.6 g, 0.50 mol) and triethyl orthoformate (148.2 g, 1.0 mol) were heated at 145° until 56 ml of ethanol had been collected by distillation. The excess triethyl orthoformate was removed by vacuum distillation. The residue was distilled to yield the formimidate required as an intermediate, bp. 142° C. (0.1 mm), mp 41°-42° C.
Anal. Calcd for C 12 H 15 NO 3 : C, 65.14; H, 6.83; N, 6.33. Found: C, 65.01; H, 6.77; N, 6.54.
(b) N'-(4-Ethoxycarbonylphenyl)-N-methyl-N-phenylformamidine
Ethyl N-(4-ethoxycarbonylphenyl formimidate (11.0 g, 0.05 mol) and N-methylaniline (5.4 g, 0.05 mol) were heated at 190° until 1.5 ml of ethanol had been collected by distillation. The viscous yellow oil was flash distilled through a short path distillation column to yield the desired product, bp. 188° C. (0.1 mm). ##STR9##
Anal. Calcd for C 17 H 18 N 2 O 2 : C, 72.33; H, 6.41; N, 9.92 Found: C, 72.22; H, 6.34; N, 9.89
EXAMPLE II
Preparation of N, N'-bis (4-Ethoxycarbonylphenyl)-N-methylformamidine
To a stirred solution of N,N'-bis(4-ethoxycarbonylphenyl)formamidine (6.8 g, 0.02 mol) in 50 ml of dimethylformamide was added 2.0 g of potassium hydroxide and 2 ml (0.02 mole) of dimethyl sulfate. The solution was stirred overnight and heated at 100° for 3 hrs. The reaction mixture was poured into 100 ml of water and the solid which precipated was collected by filtration and dried. The solid was triturated with 150 ml of benzene. The undissolved material was removed by filtration and the filtrate was concentrated to a solid residue. This solid residue was then triturated with 50 ml of chloroform. The remaining solids were removed by filtration. Concentration of the filtrate produced the desired product, mp 89°-91° C. ##STR10##
Anal. Calcd for C 20 H 22 N 2 O 4 : C, 67.78; H, 6.26; N, 7.90 Found C, 67.71; H, 6.34; N, 7.80
EXAMPLE III
Preparation of N,N-Diphenyl-N'-(4-ethoxycarbonylphenyl)formamidine
To a solution of N,N-diphenylformamide (19.7 g, 0.10 mol) in 100 ml of chloroform was added 22.8 g (0.11 mol) of phosphorus pentachloride in small portions. After the addition was completed the solution was refluxed for 1 hr. Ethyl 4-aminobenzoate (16.5 g, 0.10 mol) was added in small portions and the solution was refluxed 1 hr. The solution was poured into 100 ml of water and neutralized with concentrated ammonium hydroxide. The chloroform phase was separated, dried (MgSO 4 ), filtered and concentrated to yield a yellow oil. Purification by chromatography using silica gel/benzene yielded the desired product. ##STR11##
Anal. Calcd for C 22 H 20 N 2 O 2 : C, 76.71; H, 5.86; N, 8.13 Found: C, 76.62; H, 5.94; N, 8.38
EXAMPLE IV
Preparation of N'-(4-n-Butoxycarbonylphenyl)-N-methyl-N-phenylformamidine
Ethyl N-(n-butoxycarbonylphenyl)formimidate was prepared from n-butyl-4-aminobenzoate by a process similar to that described in Example Ia.
A mixture of ethyl N-(n-butoxycarbonylphenyl)formimidate (5.0 g, 0.02 mol) and N-methylaniline (2.1 g, 0.02 mol) were heated at 190° until 1.7 ml of ethanol had been collected by distillation. The yellow oil was flash distilled through a short path distillation column to yield the product, bp≈204° C. (0.08 mm). ##STR12##
Anal. Calcd for C 19 H 22 N 2 O 2 : C, 73.52; H, 7.15; N, 9.02 Found: C, 73.70; H, 7.15; N, 8.95
EXAMPLE V
Preparation of N-(4-n-Butoxycarbonylphenyl)-N'-(4'-ethoxycarbonylphenyl)-N-methylformamidine
Ethyl N-(4-ethoxycarbonylphenyl)formimidate (Example Ia) (6.7 g, 0.03 mol) and n-butyl 4-methylaminobenzoate (6.2 g, 0.03 mol) were heated at 190° until 1.7 ml of ethanol had been collected by distillation. The solid mass which resulted upon cooling was recrystallized from hexane to yield the product, mp 83°-85° C. ##STR13##
Anal. Calcd for C 22 H 26 N 2 O 4 : N, 7.32 Found: N, 7.23
EXAMPLE VI
Preparation of N'-(4-Ethoxycarbonylphenyl)-N-(2-methoxyphenyl)-N-methylformamidine
A mixture of ethyl N-(4-ethoxycarbonylphenyl)formimidate (Example Ia) (4.9 g, 0.022 mol) and 2-methoxy-N-methylaniline (3.2 g, 0.022 mol) were heated at 180° until 1.3 ml of ethanol had been collected by distillation. The resulting yellow oil was flash distilled to yield the desired product, bp≈200° C. (0.05 mm). ##STR14##
Anal. Calcd for C 18 H 20 N 2 O 3 : C, 69.21; H, 6.47; N, 8.96 Found C, 69.47; H, 6.49; N, 9.01
EXAMPLE VII
Preparation of N'-(4-Ethoxycarbonylphenyl)-N-(n-octyl)-N-phenylformamidine
Ethyl N-(4-ethoxycarbonylphenyl)formimidate (Example Ia) (6.6 g, 0.03 mol) and N-octylaniline (6.2 g, 0.03 mol) were heated at 180° until 1.7 ml of ethanol had been collected by distillation. The resulting pale yellow oil was flash distilled to yield the desired product, bp≈235° C. (0.05 mm). ##STR15##
Anal. Calcd for C 24 H 32 N 2 O 2 : C, 75.74; H, 8.49; N, 7.36 Found: C, 75.74; H, 8.51; N, 7.36
EXAMPLE VIII
Preparation of N'-(3-Hydroxy-4-methoxycarbonylphenyl)-N-methyl-N-phenylformamidine
Ethyl N-(3-hydroxy-4-methoxycarbonylphenyl)formimidate was prepared from n-butyl-4-aminobenzoate by a process similar to that described in Example Ia.
A mixture of ethyl N-(3-hydroxy-4-methoxycarbonylphenyl)formimidate (6.6 g, 0.03 mol) and N-methylaniline (3.2 g, 0.03 mol) were heated at 150° until 1.7 mol of ethanol had been collected by distillation. The pale yellow oil was flash distilled to yield the desired product, bp≈200° C. (0.1 mm). ##STR16##
Anal. Calcd for C 16 H 16 N.sub. 2 O 3 : C, 67.60; H, 5.66; N, 9.85 Found: C, 67.39; H, 5.91; N, 10.06
1.PublishNumber: US-4021471-A
2.Date Publish: 19770503
3.Inventor: VIRGILIO; JOSEPH A.
MANOWITZ; MILTON
4.Inventor Harmonized: VIRGILIO JOSEPH A()
MANOWITZ MILTON()
5.Country: US
6.Claims:
(en)Novel substituted formamidines are useful as ultraviolet light absorbers, the formamidines being characterized by the formula: ##STR1## wherein: R 1 represents an alkyl group containing one to five carbon atoms;
B is selected from the group consisting of H, OH, Cl or alkoxy;
R 2 represents a phenyl group or an alkyl group containing one to nine carbon atoms;
A is selected from the group consisting of H, carboalkoxy, alkoxy, alkyl, dimethylamino and halogen.
D is selected from the group consisting of H, methoxy and chlorine.
7.Description:
(en)BACKGROUND OF THE INVENTION
1. Field of the Invention
This invention relates to novel formamidines useful for protecting materials against the degradative effects of ultraviolet light.
2. The Prior Art
It is known in the art that organic materials which possess ultraviolet light absorbing properties can be added to many other organic materials to protect these materials from being degraded or damaged by ultraviolet light. For example, various polymers, plastics, resins, cosmetics, dyes, pigments, lacquors, varnishes, textiles, etc. are subject to photodegradation by sunlight or ultraviolet radiation and such materials can often be protected by treatment with chemicals which will absorb the harmful rays and convert them to relatively harmless forms of energy.
The prior art does not teach that the novel substituted formamidines of this invention possess the outstanding light absorbing properties combined with the high photostability and thermal stability as herein disclosed.
SUMMARY OF THE INVENTION
In accordance with the present invention there is provided substituted formamidines of the general structure: ##STR2## wherein: R 1 represents an alkyl group containing one to five carbon atoms:
B is selected from the group consisting of H, OH, Cl or alkoxy;
R 2 represents a phenyl group or an alkyl group containing one to nine carbon atoms;
A is selected from the group consisting of H, carboalkoxy, alkoxy, alkyl, dimethylamino and halogen.
D is selected from the group consisting of H, methoxy and chlorine.
The formamidines of this invention are particularly valuable as U.V. screening agents. As will be demonstrated they absorb over a wide range of the U.V. spectrum being particularly effective in the range from 280-370 nanometers. The formanidines are colorless and soluble in most organic solvents.
More significant and surprising is their remarkable resistance to photodegradation and thermal degradation. The formamidines of this invention are from about 5 to 30 times more resistant to photodegradation than the commercially available 2-hydroxy-4-methoxybenzophenone. The thermal stability is also illustrated by the fact that most of the formamidines were distilled at temperatures (boiling point) above 200° C. Toward the end of such distillations temperatures in the distilling vessel exceeded 300° C. without any decomposition being noted. This resistance to thermal degradation is particularly useful in applications where high temperatures are required as, for example, in the molding of plastics.
The substituted formamidines of the present invention are prepared in a number of ways, the method chosen being dependent upon the starting material available.
A preferred method utilizes as intermediates the novel formimidates of the general formula: ##STR3## wherein: R 1 and B are as defined previously and R 3 is an alkyl group of from one to five carbons. The novel formamidates, II, are prepared by reacting the corresponding 4-aminobenzoate with a trialkyl orthoformate as illustrated below. The reaction is effected by heating the reactants from ##STR4## 80° C. to 200° C. and the preferred temperature range is 130° to 160° C. The preferred procedure is to remove the alcohol which is formed during the reaction. The reaction is stopped when no more alcohol is produced. Any trialkylorthoformate may be used but it is preferred to use the commercially available triethyl or trimethyl orthoformates.
The novel formamidines, I, can be prepared by reacting the novel formimidates, II, with N-alkylanalines of general structure IV, as illustrated below: I, II, A, D, R 2 and R 3 being as previously defined. Reaction is effected by heating the reactants ##STR5## from 80° C. to 250° C., the preferred temperature range being 170° C. to 210° C. A preferred procedure is to remove the alcohol which is formed during the reaction. The reaction is stopped when no more alcohol is produced.
The N-alkylanilines, IV, can be prepared by any of the general methods known in the art. The N-alkylanilines, IV, used in this invention were prepared from the corresponding anilines, V, as shown below: ##STR6##
Any of the methods known in the art for monoacylating primary amines, alkylating amides and hydrolysing amides can be used in the preparation of the desired N-alkylanilines, IV.
Another method for preparing the novel formamidines of this invention involves the reaction of an aminobenzoate of formula III with a formamide of the general formula VI in the presence of a suitable catalyst such as phosphorous pentachloride to form the formamidines of structure I as shown below: ##STR7##
Another method for preparing the novel formamidines of this invention involves the alkylation of formamidines of general formula VII by methods known in the art. ##STR8##
Detailed procedures of each of these methods are provided herein.
The strong ultraviolet light absorbing properties of the formamidines of this invention are demonstrated by dissolving the compounds in isopropanol and determining their spectrum using a recording ultraviolet spectrophotometer. Table I lists the wavelength of maximum absorption (λ max ), the intensity of this absorption calculated as molar extinction coefficient (ε), and the λ range where ε = 5,000 or greater.
TABLE I__________________________________________________________________________ λ range (nm)Compound Name .sup.λmax (nm) ε ε >5,000__________________________________________________________________________C.sub.1 N'-(4-Ethoxycarbonylphenyl)-N-methyl- 313 26,200 280 - 350* N-phenylformamidineC.sub.2 N'-(4-Ethoxycarbonylphenyl)-N-(4-methoxyphenyl)- 312 26,300 280 - 355 N-methylformamidineC.sub.3 N,N'-Bis(4-Ethoxycarbonylphenyl)-N-methyl- 323 32,800 280 - 365 formamidineC.sub.4 N-(4-Dimethylaminophenyl)-N'-(4-ethoxy- 324 22,100 280 - 368 carbonylphenyl)-N-methylformamidineC.sub.5 N'-(4-Ethoxycarbonylphenyl)-N-(2-methoxy- 312 27,500 280 - 357 phenyl)-N-methylformamidineC.sub.6 N'-(4-Ethoxycarbonylphenyl)-N-(3,4- 312 29,500 280 - 357 dichlorophenyl)-N-methylformamidineC.sub.7 N-(4-Butoxycarbonylphenyl)-N'-(4-ethoxy- 323 36,800 280 - 368 carbonylphenyl)-N-methylformamidineC.sub.8 N'-(4-Butoxycarbonylphenyl)-N-methyl- 312 27,100 280 - 355 N-phenylformamidineC.sub.9 N'-(3-Hydroxy-4-methoxycarbonylphenyl)- 320 26,814 280 - 357 N-methyl-N-phenylformamidineC.sub.10 N-Butyl-N-phenyl-N'-(4-ethoxycarbonyl- 312 26,700 280 - 362 phenyl)formamidineC.sub.11 N'-(4-Ethoxycarbonylphenyl)-N-(n-octyl)- 314 28,300 280 - 357 N-phenylformamidineC.sub.12 N,N-Diphenyl-N'-(4-ethoxycarbonylphenyl)- 317 25,300 280 - 357 formamidineC.sub.13 N'-(4-Ethoxycarbonyl-3-methoxyphenyl)- 320 27,000 280 - 358 N'-methyl-N-phenylformamidineC.sub.14 N'-(4-Isopropoxycarbonylphenyl)-N- 312 26,800 280 - 356 methyl-N-phenylformamidineC.sub.15 N'-(4-Ethoxycarbonylphenyl)-N-methyl-N-(p- 313 27,000 280 - 357 ethylphenylformamidineC.sub.16 N'-(2-Chloro-4-methoxycarbonylphenyl)-N- 318 25,800 280 - 360 methyl-N-phenylformamidine__________________________________________________________________________ *Only wavelengths above 280 nm were included.
The photostability of the formamidines of this invention was demonstrated in accelerated irradiation tests by exposing isopropanol solution of the compounds in pyrex flasks under a Hanovid lamp 679A (450 watts). Aliquots of these solutions were periodically examined spectrophotometrically to determine their rate of photodegradation. Results of these tests are listed in Table II including the test data for a commercially used hydroxybenzophenone type screening agent.
TABLE II______________________________________ Percent Degradation Exposure Time (hours)Compound O 8 16 24______________________________________C.sub.1 0 7 7 7C.sub.2 0 6 9 9C.sub.3 0 0 2 3C.sub.4 0 4 8 22C.sub.5 0 3 5 19C.sub.6 0 1 8 16C.sub.7 0 2 3 9C.sub.8 0 1 1 9C.sub.9 0 3 5 10C.sub.10 0 5 7 13C.sub.11 0 2 7 15C.sub.12 0 2 5 16 2-Hydroxy- 4-methoxy- benzophe- none 0 2 75 100______________________________________
The ability of the novel formamidines of this mixture to retard the discoloration of plastic films when incorporated therein is shown by the following described test and results.
Plastic films containing 0.4% by weight of the novel formamidines of this invention were prepared from a non-plasticized polyvinylchloride (87%) polyvinylacetate (13%) resin. The films were exposed to a Hanovia lamp 679A (450 watts) and periodically examined for discoloration. Results of these tests are listed in Table III using the following commercial ratings: o-no discoloration, 1-trace, 2-slight, 3-moderate, 4-severe.
TABLE III______________________________________ Discoloration Exposure Period (hours)Compound 0 8 16 24 48 80______________________________________Control 0 2 3 3 4 4C.sub.1 0 0 0 1 2 2C.sub.2 0 1 1 1 2 2C.sub.3 0 1 1 2 3 3C.sub.5 0 0 1 1 2 2C.sub.7 0 0 1 1 2 2C.sub.8 0 0 0 0 1 2C.sub.9 0 0 0 0 1 2______________________________________
The ability of the novel compound of this invention to retard the fading of dyes when incorporated therein is shown by the following described test and results.
Isopropanol solutions of the blue dye FD&C Blue No. 1, (H. Kohnstamm & Co.) containing 0.01% of a UV Absorber Formamidine of the invention were exposed to UV irradiation from G.E. fluorescent lamps F40BL. These solutions were periodically examined spectrophotometrically to determine the degree to which the dye has faded. The results are given in Table IV.
TABLE IV______________________________________FD&C Blue No. 1 Percent Degradation ofUV Absorber Versus Exposure Time (days)______________________________________ 14 20Control 100Tinuvin P 60 80C.sub.2 7 7C.sub.5 20 20C.sub.7 7 7C.sub.9 60 67______________________________________
The following examples are presented to provide a more detailed explanation of the present invention and are intended as illustrations and not limitations of the invention. Unless otherwise stated herein, the temperatures are in degrees Centigrade and all parts are by weight.
EXAMPLE I
Preparation of N'-(4-Ethoxycarbonylphenyl)-N-methyl-N-phenylformamidine
a. Ethyl (4-ethoxycarbonylphenyl)formimidate (a)
Ethyl 4-aminobenzoate (82.6 g, 0.50 mol) and triethyl orthoformate (148.2 g, 1.0 mol) were heated at 145° until 56 ml of ethanol had been collected by distillation. The excess triethyl orthoformate was removed by vacuum distillation. The residue was distilled to yield the formimidate required as an intermediate, bp. 142° C. (0.1 mm), mp 41°-42° C.
Anal. Calcd for C 12 H 15 NO 3 : C, 65.14; H, 6.83; N, 6.33. Found: C, 65.01; H, 6.77; N, 6.54.
(b) N'-(4-Ethoxycarbonylphenyl)-N-methyl-N-phenylformamidine
Ethyl N-(4-ethoxycarbonylphenyl formimidate (11.0 g, 0.05 mol) and N-methylaniline (5.4 g, 0.05 mol) were heated at 190° until 1.5 ml of ethanol had been collected by distillation. The viscous yellow oil was flash distilled through a short path distillation column to yield the desired product, bp. 188° C. (0.1 mm). ##STR9##
Anal. Calcd for C 17 H 18 N 2 O 2 : C, 72.33; H, 6.41; N, 9.92 Found: C, 72.22; H, 6.34; N, 9.89
EXAMPLE II
Preparation of N, N'-bis (4-Ethoxycarbonylphenyl)-N-methylformamidine
To a stirred solution of N,N'-bis(4-ethoxycarbonylphenyl)formamidine (6.8 g, 0.02 mol) in 50 ml of dimethylformamide was added 2.0 g of potassium hydroxide and 2 ml (0.02 mole) of dimethyl sulfate. The solution was stirred overnight and heated at 100° for 3 hrs. The reaction mixture was poured into 100 ml of water and the solid which precipated was collected by filtration and dried. The solid was triturated with 150 ml of benzene. The undissolved material was removed by filtration and the filtrate was concentrated to a solid residue. This solid residue was then triturated with 50 ml of chloroform. The remaining solids were removed by filtration. Concentration of the filtrate produced the desired product, mp 89°-91° C. ##STR10##
Anal. Calcd for C 20 H 22 N 2 O 4 : C, 67.78; H, 6.26; N, 7.90 Found C, 67.71; H, 6.34; N, 7.80
EXAMPLE III
Preparation of N,N-Diphenyl-N'-(4-ethoxycarbonylphenyl)formamidine
To a solution of N,N-diphenylformamide (19.7 g, 0.10 mol) in 100 ml of chloroform was added 22.8 g (0.11 mol) of phosphorus pentachloride in small portions. After the addition was completed the solution was refluxed for 1 hr. Ethyl 4-aminobenzoate (16.5 g, 0.10 mol) was added in small portions and the solution was refluxed 1 hr. The solution was poured into 100 ml of water and neutralized with concentrated ammonium hydroxide. The chloroform phase was separated, dried (MgSO 4 ), filtered and concentrated to yield a yellow oil. Purification by chromatography using silica gel/benzene yielded the desired product. ##STR11##
Anal. Calcd for C 22 H 20 N 2 O 2 : C, 76.71; H, 5.86; N, 8.13 Found: C, 76.62; H, 5.94; N, 8.38
EXAMPLE IV
Preparation of N'-(4-n-Butoxycarbonylphenyl)-N-methyl-N-phenylformamidine
Ethyl N-(n-butoxycarbonylphenyl)formimidate was prepared from n-butyl-4-aminobenzoate by a process similar to that described in Example Ia.
A mixture of ethyl N-(n-butoxycarbonylphenyl)formimidate (5.0 g, 0.02 mol) and N-methylaniline (2.1 g, 0.02 mol) were heated at 190° until 1.7 ml of ethanol had been collected by distillation. The yellow oil was flash distilled through a short path distillation column to yield the product, bp≈204° C. (0.08 mm). ##STR12##
Anal. Calcd for C 19 H 22 N 2 O 2 : C, 73.52; H, 7.15; N, 9.02 Found: C, 73.70; H, 7.15; N, 8.95
EXAMPLE V
Preparation of N-(4-n-Butoxycarbonylphenyl)-N'-(4'-ethoxycarbonylphenyl)-N-methylformamidine
Ethyl N-(4-ethoxycarbonylphenyl)formimidate (Example Ia) (6.7 g, 0.03 mol) and n-butyl 4-methylaminobenzoate (6.2 g, 0.03 mol) were heated at 190° until 1.7 ml of ethanol had been collected by distillation. The solid mass which resulted upon cooling was recrystallized from hexane to yield the product, mp 83°-85° C. ##STR13##
Anal. Calcd for C 22 H 26 N 2 O 4 : N, 7.32 Found: N, 7.23
EXAMPLE VI
Preparation of N'-(4-Ethoxycarbonylphenyl)-N-(2-methoxyphenyl)-N-methylformamidine
A mixture of ethyl N-(4-ethoxycarbonylphenyl)formimidate (Example Ia) (4.9 g, 0.022 mol) and 2-methoxy-N-methylaniline (3.2 g, 0.022 mol) were heated at 180° until 1.3 ml of ethanol had been collected by distillation. The resulting yellow oil was flash distilled to yield the desired product, bp≈200° C. (0.05 mm). ##STR14##
Anal. Calcd for C 18 H 20 N 2 O 3 : C, 69.21; H, 6.47; N, 8.96 Found C, 69.47; H, 6.49; N, 9.01
EXAMPLE VII
Preparation of N'-(4-Ethoxycarbonylphenyl)-N-(n-octyl)-N-phenylformamidine
Ethyl N-(4-ethoxycarbonylphenyl)formimidate (Example Ia) (6.6 g, 0.03 mol) and N-octylaniline (6.2 g, 0.03 mol) were heated at 180° until 1.7 ml of ethanol had been collected by distillation. The resulting pale yellow oil was flash distilled to yield the desired product, bp≈235° C. (0.05 mm). ##STR15##
Anal. Calcd for C 24 H 32 N 2 O 2 : C, 75.74; H, 8.49; N, 7.36 Found: C, 75.74; H, 8.51; N, 7.36
EXAMPLE VIII
Preparation of N'-(3-Hydroxy-4-methoxycarbonylphenyl)-N-methyl-N-phenylformamidine
Ethyl N-(3-hydroxy-4-methoxycarbonylphenyl)formimidate was prepared from n-butyl-4-aminobenzoate by a process similar to that described in Example Ia.
A mixture of ethyl N-(3-hydroxy-4-methoxycarbonylphenyl)formimidate (6.6 g, 0.03 mol) and N-methylaniline (3.2 g, 0.03 mol) were heated at 150° until 1.7 mol of ethanol had been collected by distillation. The pale yellow oil was flash distilled to yield the desired product, bp≈200° C. (0.1 mm). ##STR16##
Anal. Calcd for C 16 H 16 N.sub. 2 O 3 : C, 67.60; H, 5.66; N, 9.85 Found: C, 67.39; H, 5.91; N, 10.06
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