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1.ApplicationNumber: US-15781061-A
1.PublishNumber: US-3219655-A
2.Date Publish: 19651123
3.Inventor: RONCO KARL
4.Inventor Harmonized: KARL RONCO()
5.Country: US
6.Claims:
7.Description:
(en)United States Patent Oilfice 3,219,655 Patented Nov. 23, 1955 This invention provides azo-dyestuifs which are free from groups imparting solubility in water and correspond to the general formula:
Gama oin which R represents a benzene residue which is bound in the 1-position to the azo linkage and in the 3-position to the carbonyl group, and in 6-position contains a halogen atom, an alkoxy group or a phenoxy group R represents a naphthalene residue to which the azo linkage, the hydroxyl group and the CONH group are bound in the l-, 2 and 3- positions, respectively. X and Y each represent a halogen atom or alkyl group, and when X is a halogen atom, Y may also represent an alkoxy group, and the benzene residue B may contain further substituents.
The invention also provides a process for the manufacture of the aforesaid azddyestutfs, wherein one molecular proportion of a carboxylic acid halide which is free from groups imparting solubility in water and corresponds to the formula:
OHal
in which R represents a benzene residue which is bound in the 1-position to the azo linkage and in the 3-position to the carbonyl group and contains in the 6-position a halogen atom or alkoxy or penoxy group, R represents a a naphthalene residue to which the azo linkage, the hydroxyl group and the carboxylic acid halide group are bound in the 1-, 2- and 3-positions repectively, is reacted with two molecular proportions of an amine of the formula:
The azo-carboxylic acids, from which the acid halides of the above Formula 1 are obtained can be made coupling the diazo-compound of a meta-aminabenzene carboxylic acid with a 2:3-hydroxynapthoic acid.
As meta-arninobenzene carboxylic acids are advantageously used those of the formula:
in which Z represents a halogen atom or an alkoxy or phenoxy group, and Z represents a hydrogen or halogen atom. Especially useful is the aminobenzene carboxylic acid of the formula:
The 2:3-hydroxynaphthoic acid used as coupling component may be substituted in the benzene ring that does not contain the carboxylic acid group, for example, by a halogen atom, especially a bromine atom in the 6-position, or by an alkoxy or alkyl group. Owing to its ready availability, it is of advantage to use the 2:3-hydroxynaphthoic acid itself.
The aZo-dicarboxylic acids so obtained are treated with an agent capable of converting carboxylic acids into their halides, for example, into their chlorides or bro mides. Such agents are more especially phosphorus halides, such as phosphorus pentabromide, phosphorus trichloride or phosphorus pentachloride, or phosphorus oxyhalides, or preferably thionyl chloride.
The treatment with the above acid-halogenating agents is advantageously carried out in an inert organic solvent, such as chlorobenzene, for example, monoor di-chlorobenzene or toluene, Xylene or nitrobenzene.
For the preparation of the carboxylic acid halides it is generally advantageous, since the azo-dicarboxylic acids are prepared in an aqueous medium, first to dry the acids or to free them from water by azeotropic distillation with an organic solvent. The azeotropic drying process may, if desired, be carried out immediately before the treatment with the acid-halogenating agent.
The new dyestuffs are valuable red pigments. Especially valuable are the dyestuffs of the formula:
OH Ili in which X and Y each represent a chlorine atom or a methyl group and Z Z and B have the meanings given above. These dyestuffs are distinguished by their especially high colouring power, their especially good fastness to light and migration, their high degree of thermo-stability, and their good resistance to solvents.
The pigments of the invention are useful for a very wide variety of application of pigments, for example, in a finely divided form for colouring artificial silk and viscose, cellulse ethers and esters, super-polyamides, or super-polyeruthanes or polyesters in spinning masses, or for colouring lacquers, lacquer-forming substances, solutions and products of acetyl-cellulose, nitro-cellu-lose, natural resins or synthetic resins, such as polyemrisation or condensation resins such, for example, as aminoplasts, alkyd resins, phenoplasts, polystyrene, polyvinyl chloride, polyethylene, polypropoylene, polyacryl, gums, casein, silicones and silicone resins. They may also be used with advantage in the manufacture of dystuffs, cosmetics and laminated sheet materials.
The following examples illustrate the invention, the parts and percentages being by weight:
Example 1 20.3 parts of the dyestufi obtained by coupling diazotized -arnino-2:4-dichlorobenzoic acid with 2:3-hydroxynaphthoic acid are stirred for 3 hours at 115-120" C. with 250 parts of ortho-dichlorobenzene, 0.5 part of dimethyl-formamide and 12 parts of thionyl chloride. The reaction mixture is then cooled and the uniformly crystalline dicarboxylic acid chloride of the dyestuff obtained is filtered off, and then dried at 55-60 C. under vacuum, 22 parts of the di-acid chloride so obtained are stirred into 1000 parts of ortho-dichlorobenzene at 100 C. A warm solution of 28.5 parts of 2:5-dichloro-4-benzoylaminoaniline in 300 parts of ortho-dichlorobenzene are then poured into the mixture. The mixture is then stirred for 16 hours at l40145 C. The pigment so obtained is filtered off at 120 C., washed with hot ortho-dichlorobenzene, hot benzene and methanol, and dried at 7080 C. in vacuo. The pigment dystufi so obtained is a soft grained scarlet-red powder which colours polyvinyl foils scarlet-red tints of excellent fastness to light and migration. The dystuif corresponds to the following formula:
Example 2 parts of polyvinyl chloride, 35 parts of dioctyl phthalate and 0.2 part of the dyestuff obtained in Example 1 are stirred together and then rolled backwards and forwards for 7 minutes at C. on a two-roller callender. The foil so obtained has a scarlet-red colour of very good fastness to light and migration.
In the following table are given further pigment dyestuifs which can be obtained by the method described above and which also have very good properties of fastness. Column 1 gives the diazo components, column II the coupling components, column III the amines with which the azo-dicarboxylic acid halides are condensed, and column IV the colours of foils of polyvinyl chloride coloured with pigments.
No. I 11 111 IV 1 5-amino-2,4-diehlorobenz0ic acid 2:3-hydr0xynaphthoic acid 2:5-dimethyl-4-benzoylaminoaniline Scarlet red. 2 do do 5-chloro-4-benzoylamino-Z-methyoxyaniline Do. 3 dn d 2:5-diehloro-4(4-ehloro)-benzoylarninoaniline Do. 4 dn do 2:5-di1c hloro4(2:4-dieh1oro)benzoylamino- D0.
anl me. 5 do d o 2:5-di1methyl-4(2:5-dieh1oro)-benzoy1amino- Do.
am ine. 6 d n 2:5-diehloro-4(2:5-dichloro)-benz0ylamin0- Bordeaux.
2. me. 7 do 2:5-di1nethyl-4(4-chloro)-benzoylaminoaniline. Red. 8 do do 2:5-d:imethyl-4(2:4-dichloro) benxoylamino Scarlet red.
- am me. 9. .d n d o Z-rgngfihoxy-at (4-chloro) -benz oylamino-S-chlor- D 0.
me. 10 5-amino-2A-dichloro benzoic acid d0 z-methoxyt-(a-naphthoylamino)-5-ch1orani1ine Do. 11. fi-amiiuo-4-methoxy-2-ehlorobenzoic d0 2-methoxy-4-benzoylamin0-5-chloroaniline Bluish red.
aci 12 do d 2:5-diehloro-4-benzoylaaninoaniline Bordeaux. 1'; do do 2:fi-dimethyli benzoylaminoaniline Bluish red. 14 5-ann'no-4-methoxy-2-ch1orobenzoic d0 2:5-dichloro-4(4-ehloro)-benzoylaminoaniline Red.
aer 15 3-amino-4(4-eh10ro)-phenoxybenzoic d0 2-methoxyi-benzoylamino-fi-ehloraniline Red.
2-ehloro-4-benzoylamino-5-methoxyani1ine Scarlet red. 2:5-dichloro-4-benzoylaminoaniline Red. do do Scarlet red Z-methoxydbenzoylamino-5-ch10raniline Bordeaux. d 2-ch1or0-4-benzoylamino-S-methoxyaniline Red. dn 2:5-dieh1oro-4-benzoylaminoaniline Bordeaux. n 2:5-dimethy1-4-benzoylaminoaniline Ruby. dn 2:5-dichl0ro-4- (4-ehloro)-benzoylaminoaniline Red. n 2:5-dii1ehloro-4(2:5-dichl0ro)-benz0y1amino Bordeaux.
an me. 2:5-dichloro-4(2:4-diehloro) benzoylamino Scarlet red.
aniline. 2:5-dichloro-4-benzoylaminoaniline Bordeaux. 2:5-dimethylt-benzoylaminoaniline Ruby. 2:5-difilliloro-4-(2:4-diehloro)-beuzoy1amino- Red.
an e.
N o. I III IV 29 ,do d 2:5-dimethyl-4-(4'-chloro)-henzoylarninoaniline Ruby. 80 do d 2:5-diil1nethyl-4-(2:4dichl0ro)-benzoylamlno- Red.
an me. 4-fiuorO-3-aminoben7oic d z-rnethoxyt-benzoylamino-E-chloraniline Scarlet Red. do "do 2-chloro-4-benzoylamino-S-methoxyaniline Do. ,do do 2:5-dichloro-4-benzoylamlnoaniline Do. do 7 2:5-dimethyll-benzoylaminoaniline D0. 4-chloro-3-aminobenzoic acid 2-methoxy-4-benzoylamin o--chloroaniline Do. do 2-chloro-4-benzoylamino-5-methoxyaniline Do. 2:5-diehlorul-benzoylaminoaniline D0. 2:5-dimethyl-4benzoyl Scarlet red. 2:5-dichl0ro-4-(4 chlor0) -benzoy1aminoaniline Orange. 2zfi-qflchlorw(2:4-dich1or0)-benzoy1hmino- D0.
am me. 2:5-di1nethyl-4-(4-ch1oro)-benzoy1aminoaniline Scarlet red. 2:5-d i1rnethy1-4-(2:5-dichlor0)-benzoylamino- Red.
an! me. 2:5-dichloro-4-benzoylamlnoaniline Scarlet red. 2methoxy-4-benzcylamino-5-chloraniline Red. 45 n 2zE-diehlor0-4-benz0y1amin0aniline Orange, 46; do 2:5-dimcthylA-benzoylaminoaniline Scarlet red. 47 -methoxy-Zi-aminobenzoic acid 2:5'dimethyl--benzoylaminonniline Ruby. 48 ,do I 2:5-dichloroi-benzoylaminozmiline. Do. 49 do 2:5-dii1chlor 0-4 (2:4-dichloro) -benzoylamino- Violet.
an me. 50 "do 2:5-dimethyl-4-(4-chloro)-benzoylaminoanlllne Ruby. 51 -do 2:5-di1iln1ethyl-4 (2:5'-dicl1loro) -beuzoy1amino- B ordeaux.
am e. 2,5-dichloro-4-benzoylaminoaniline Orange. 2,5-diChX0-4-(4'43111010)-b8IlZOY1aII1lIlOaI1l1lIl8. D o. 2,5-diiln1ethyl-4(2,5-dicl1l0r0)-benz0ylamino- Do.
an me. 2,5-dimethyl-4-henzoylnmlnoaniline Brown orange. 2,fi-dimethy1-4(4-chloro)-benzoylaminoeniline.. Red orange.
What I claim is: 1. An azo-dyestulf of the formula r6 N l O H X 1 X -0 oNE-O-NHC o@ chlorine and the group of the formula and Z is a member selected from the group consisting of hydrogen and the group of the Formula 2, and wherein only one of the substituents Z and Z represents the group of the Formula 2.
2. The dyestuff of the formula N C1 E31 ,l ONE NHW I 1 -CONH 3. The dyestufl of the formula 4. The dyestutf of the formula -0 ONE 5. The dyestuff of the formula T 7. The dyestufl of the formula u OCHa References Cited by the Examiner UNITED STATES PATENTS 2,oss ,726 8/1937 Sexton 260--203 CHARLES B. PARKER, Primary Examiner.
| v ONHQ-NHC 00-01 0H r0113 1 10 -c ONHQNHC 00-01
1.PublishNumber: US-3219655-A
2.Date Publish: 19651123
3.Inventor: RONCO KARL
4.Inventor Harmonized: KARL RONCO()
5.Country: US
6.Claims:
7.Description:
(en)United States Patent Oilfice 3,219,655 Patented Nov. 23, 1955 This invention provides azo-dyestuifs which are free from groups imparting solubility in water and correspond to the general formula:
Gama oin which R represents a benzene residue which is bound in the 1-position to the azo linkage and in the 3-position to the carbonyl group, and in 6-position contains a halogen atom, an alkoxy group or a phenoxy group R represents a naphthalene residue to which the azo linkage, the hydroxyl group and the CONH group are bound in the l-, 2 and 3- positions, respectively. X and Y each represent a halogen atom or alkyl group, and when X is a halogen atom, Y may also represent an alkoxy group, and the benzene residue B may contain further substituents.
The invention also provides a process for the manufacture of the aforesaid azddyestutfs, wherein one molecular proportion of a carboxylic acid halide which is free from groups imparting solubility in water and corresponds to the formula:
OHal
in which R represents a benzene residue which is bound in the 1-position to the azo linkage and in the 3-position to the carbonyl group and contains in the 6-position a halogen atom or alkoxy or penoxy group, R represents a a naphthalene residue to which the azo linkage, the hydroxyl group and the carboxylic acid halide group are bound in the 1-, 2- and 3-positions repectively, is reacted with two molecular proportions of an amine of the formula:
The azo-carboxylic acids, from which the acid halides of the above Formula 1 are obtained can be made coupling the diazo-compound of a meta-aminabenzene carboxylic acid with a 2:3-hydroxynapthoic acid.
As meta-arninobenzene carboxylic acids are advantageously used those of the formula:
in which Z represents a halogen atom or an alkoxy or phenoxy group, and Z represents a hydrogen or halogen atom. Especially useful is the aminobenzene carboxylic acid of the formula:
The 2:3-hydroxynaphthoic acid used as coupling component may be substituted in the benzene ring that does not contain the carboxylic acid group, for example, by a halogen atom, especially a bromine atom in the 6-position, or by an alkoxy or alkyl group. Owing to its ready availability, it is of advantage to use the 2:3-hydroxynaphthoic acid itself.
The aZo-dicarboxylic acids so obtained are treated with an agent capable of converting carboxylic acids into their halides, for example, into their chlorides or bro mides. Such agents are more especially phosphorus halides, such as phosphorus pentabromide, phosphorus trichloride or phosphorus pentachloride, or phosphorus oxyhalides, or preferably thionyl chloride.
The treatment with the above acid-halogenating agents is advantageously carried out in an inert organic solvent, such as chlorobenzene, for example, monoor di-chlorobenzene or toluene, Xylene or nitrobenzene.
For the preparation of the carboxylic acid halides it is generally advantageous, since the azo-dicarboxylic acids are prepared in an aqueous medium, first to dry the acids or to free them from water by azeotropic distillation with an organic solvent. The azeotropic drying process may, if desired, be carried out immediately before the treatment with the acid-halogenating agent.
The new dyestuffs are valuable red pigments. Especially valuable are the dyestuffs of the formula:
OH Ili in which X and Y each represent a chlorine atom or a methyl group and Z Z and B have the meanings given above. These dyestuffs are distinguished by their especially high colouring power, their especially good fastness to light and migration, their high degree of thermo-stability, and their good resistance to solvents.
The pigments of the invention are useful for a very wide variety of application of pigments, for example, in a finely divided form for colouring artificial silk and viscose, cellulse ethers and esters, super-polyamides, or super-polyeruthanes or polyesters in spinning masses, or for colouring lacquers, lacquer-forming substances, solutions and products of acetyl-cellulose, nitro-cellu-lose, natural resins or synthetic resins, such as polyemrisation or condensation resins such, for example, as aminoplasts, alkyd resins, phenoplasts, polystyrene, polyvinyl chloride, polyethylene, polypropoylene, polyacryl, gums, casein, silicones and silicone resins. They may also be used with advantage in the manufacture of dystuffs, cosmetics and laminated sheet materials.
The following examples illustrate the invention, the parts and percentages being by weight:
Example 1 20.3 parts of the dyestufi obtained by coupling diazotized -arnino-2:4-dichlorobenzoic acid with 2:3-hydroxynaphthoic acid are stirred for 3 hours at 115-120" C. with 250 parts of ortho-dichlorobenzene, 0.5 part of dimethyl-formamide and 12 parts of thionyl chloride. The reaction mixture is then cooled and the uniformly crystalline dicarboxylic acid chloride of the dyestuff obtained is filtered off, and then dried at 55-60 C. under vacuum, 22 parts of the di-acid chloride so obtained are stirred into 1000 parts of ortho-dichlorobenzene at 100 C. A warm solution of 28.5 parts of 2:5-dichloro-4-benzoylaminoaniline in 300 parts of ortho-dichlorobenzene are then poured into the mixture. The mixture is then stirred for 16 hours at l40145 C. The pigment so obtained is filtered off at 120 C., washed with hot ortho-dichlorobenzene, hot benzene and methanol, and dried at 7080 C. in vacuo. The pigment dystufi so obtained is a soft grained scarlet-red powder which colours polyvinyl foils scarlet-red tints of excellent fastness to light and migration. The dystuif corresponds to the following formula:
Example 2 parts of polyvinyl chloride, 35 parts of dioctyl phthalate and 0.2 part of the dyestuff obtained in Example 1 are stirred together and then rolled backwards and forwards for 7 minutes at C. on a two-roller callender. The foil so obtained has a scarlet-red colour of very good fastness to light and migration.
In the following table are given further pigment dyestuifs which can be obtained by the method described above and which also have very good properties of fastness. Column 1 gives the diazo components, column II the coupling components, column III the amines with which the azo-dicarboxylic acid halides are condensed, and column IV the colours of foils of polyvinyl chloride coloured with pigments.
No. I 11 111 IV 1 5-amino-2,4-diehlorobenz0ic acid 2:3-hydr0xynaphthoic acid 2:5-dimethyl-4-benzoylaminoaniline Scarlet red. 2 do do 5-chloro-4-benzoylamino-Z-methyoxyaniline Do. 3 dn d 2:5-diehloro-4(4-ehloro)-benzoylarninoaniline Do. 4 dn do 2:5-di1c hloro4(2:4-dieh1oro)benzoylamino- D0.
anl me. 5 do d o 2:5-di1methyl-4(2:5-dieh1oro)-benzoy1amino- Do.
am ine. 6 d n 2:5-diehloro-4(2:5-dichloro)-benz0ylamin0- Bordeaux.
2. me. 7 do 2:5-di1nethyl-4(4-chloro)-benzoylaminoaniline. Red. 8 do do 2:5-d:imethyl-4(2:4-dichloro) benxoylamino Scarlet red.
- am me. 9. .d n d o Z-rgngfihoxy-at (4-chloro) -benz oylamino-S-chlor- D 0.
me. 10 5-amino-2A-dichloro benzoic acid d0 z-methoxyt-(a-naphthoylamino)-5-ch1orani1ine Do. 11. fi-amiiuo-4-methoxy-2-ehlorobenzoic d0 2-methoxy-4-benzoylamin0-5-chloroaniline Bluish red.
aci 12 do d 2:5-diehloro-4-benzoylaaninoaniline Bordeaux. 1'; do do 2:fi-dimethyli benzoylaminoaniline Bluish red. 14 5-ann'no-4-methoxy-2-ch1orobenzoic d0 2:5-dichloro-4(4-ehloro)-benzoylaminoaniline Red.
aer 15 3-amino-4(4-eh10ro)-phenoxybenzoic d0 2-methoxyi-benzoylamino-fi-ehloraniline Red.
2-ehloro-4-benzoylamino-5-methoxyani1ine Scarlet red. 2:5-dichloro-4-benzoylaminoaniline Red. do do Scarlet red Z-methoxydbenzoylamino-5-ch10raniline Bordeaux. d 2-ch1or0-4-benzoylamino-S-methoxyaniline Red. dn 2:5-dieh1oro-4-benzoylaminoaniline Bordeaux. n 2:5-dimethy1-4-benzoylaminoaniline Ruby. dn 2:5-dichl0ro-4- (4-ehloro)-benzoylaminoaniline Red. n 2:5-dii1ehloro-4(2:5-dichl0ro)-benz0y1amino Bordeaux.
an me. 2:5-dichloro-4(2:4-diehloro) benzoylamino Scarlet red.
aniline. 2:5-dichloro-4-benzoylaminoaniline Bordeaux. 2:5-dimethylt-benzoylaminoaniline Ruby. 2:5-difilliloro-4-(2:4-diehloro)-beuzoy1amino- Red.
an e.
N o. I III IV 29 ,do d 2:5-dimethyl-4-(4'-chloro)-henzoylarninoaniline Ruby. 80 do d 2:5-diil1nethyl-4-(2:4dichl0ro)-benzoylamlno- Red.
an me. 4-fiuorO-3-aminoben7oic d z-rnethoxyt-benzoylamino-E-chloraniline Scarlet Red. do "do 2-chloro-4-benzoylamino-S-methoxyaniline Do. ,do do 2:5-dichloro-4-benzoylamlnoaniline Do. do 7 2:5-dimethyll-benzoylaminoaniline D0. 4-chloro-3-aminobenzoic acid 2-methoxy-4-benzoylamin o--chloroaniline Do. do 2-chloro-4-benzoylamino-5-methoxyaniline Do. 2:5-diehlorul-benzoylaminoaniline D0. 2:5-dimethyl-4benzoyl Scarlet red. 2:5-dichl0ro-4-(4 chlor0) -benzoy1aminoaniline Orange. 2zfi-qflchlorw(2:4-dich1or0)-benzoy1hmino- D0.
am me. 2:5-di1nethyl-4-(4-ch1oro)-benzoy1aminoaniline Scarlet red. 2:5-d i1rnethy1-4-(2:5-dichlor0)-benzoylamino- Red.
an! me. 2:5-dichloro-4-benzoylamlnoaniline Scarlet red. 2methoxy-4-benzcylamino-5-chloraniline Red. 45 n 2zE-diehlor0-4-benz0y1amin0aniline Orange, 46; do 2:5-dimcthylA-benzoylaminoaniline Scarlet red. 47 -methoxy-Zi-aminobenzoic acid 2:5'dimethyl--benzoylaminonniline Ruby. 48 ,do I 2:5-dichloroi-benzoylaminozmiline. Do. 49 do 2:5-dii1chlor 0-4 (2:4-dichloro) -benzoylamino- Violet.
an me. 50 "do 2:5-dimethyl-4-(4-chloro)-benzoylaminoanlllne Ruby. 51 -do 2:5-di1iln1ethyl-4 (2:5'-dicl1loro) -beuzoy1amino- B ordeaux.
am e. 2,5-dichloro-4-benzoylaminoaniline Orange. 2,5-diChX0-4-(4'43111010)-b8IlZOY1aII1lIlOaI1l1lIl8. D o. 2,5-diiln1ethyl-4(2,5-dicl1l0r0)-benz0ylamino- Do.
an me. 2,5-dimethyl-4-henzoylnmlnoaniline Brown orange. 2,fi-dimethy1-4(4-chloro)-benzoylaminoeniline.. Red orange.
What I claim is: 1. An azo-dyestulf of the formula r6 N l O H X 1 X -0 oNE-O-NHC o@ chlorine and the group of the formula and Z is a member selected from the group consisting of hydrogen and the group of the Formula 2, and wherein only one of the substituents Z and Z represents the group of the Formula 2.
2. The dyestuff of the formula N C1 E31 ,l ONE NHW I 1 -CONH 3. The dyestufl of the formula 4. The dyestutf of the formula -0 ONE 5. The dyestuff of the formula T 7. The dyestufl of the formula u OCHa References Cited by the Examiner UNITED STATES PATENTS 2,oss ,726 8/1937 Sexton 260--203 CHARLES B. PARKER, Primary Examiner.
| v ONHQ-NHC 00-01 0H r0113 1 10 -c ONHQNHC 00-01
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