1.ApplicationNumber: US-32766952-A
1.PublishNumber: US-2730554-A
2.Date Publish: 19560110
3.Inventor: SCHETTY GUIDO
STAMMBACH WALTER
MODEL ERNST

4.Inventor Harmonized: GUIDO SCHETTY()
WALTER STAMMBACH()
ERNST MODEL()

5.Country: US
6.Claims:

7.Description:
(en)2,730,554 Patented Jan. 10, 1956 GERMICIDAL DIPHENYL METHANE COMPOUNDS Guido Schetty, Walter Stammbach and Ernst Model,
Basel, Switzerland, assignors to J. R. Geigy A. G., Basel, Switzerland, a Swiss firm Application December 23, 1952, Serial No. 327,669
Claims priority, application Switzerland December 29, 1951 3 Claims. (Cl. 260-619) No Drawing.
The present invention concerns the production of very active germicidal diphenyl methane derivatives which have a wide range of action.
It has been found that by condensation by methods known per se of 4-halogen-l-hydroxybenzenes, of which A the 2- and G-positions are free and which compounds are Hal X: X; Hal
In this formula, "in both benzene rings, Hal represents halogen, one X represents hydrogen or halogen and the other X represents halogen or the trifiuoromethyl group.
The new 2.2-dihydroxydiphenyl methane compounds have an excellent germicidal action and are distinguished from other similar previously known compounds by a superior range of activity.
For economical reasons, advantageously chlorine atoms, however also bromine atoms, come into consideration as halogen substituents in the 4-halogen-1-hydroxybenzenes of the above definition usable according to the present invention. As suitable phenols may be named: 3.4-dichloro-l-hydroxybenzene, 3.4.5-trichloro--l-hydroxybenzene, 3.4- dibromo 1 hydroxybenzene, 3-chloro4- bromo-- and 3-bromo-4-chloro-1-hydroxybenzene, and in particular, 3-trifluoromethyl-4-chloro-l-hydroxybenzene. Of the 4-chlorophenols usable according to the present invention which are of practical interest, 3.4-dichlorophenol produces more active condensation products than 3.4.5-trichlorophenol and 3-trifluoromethyl-4-chlorophen01 produces themost valuable condensation product according to the present invention both with regard to activity and also range of action.
The condensation of the 4-halogen phenols usable according to this invention with formaldehyde or with agents giving of]? formaldehyde is performed by methods known per se, for example in concentrated sulphuric acid in the presence or absence of organic solvents or diluents such as lower alcohols. Concentrated aqueous solutions of formaldehyde or of paraformaldehyde come into question as formaldehyde or agents giving off formaldehyde.
In contrast to the known halogenated 2.2-dihydroxydiphenyl methane compounds which either have no free o-position to the hydroxyl group or have no neighbouring position to .the halogen atom in p-position occupied, the new diphenyl methane derivatives according to this invention have the advantage of an increased activity and, in particular, a superior range of action as they are also active against certain gram-negative bacteria.
The 2.2'-dihydroxydiphenyl methane derivatives according to the present invention are white, clearly crystalline powders which have no smell and most of which have a definite melting point. They dissolve a little in water, but well in lower alcohols and ketones such as ethyl alcohol or acetone. In water, their mono-alkali salts only dissolve a little but their di-alkali salts dissolve well. For disinfection purposes the new diphenyl methane compounds are used in aqueous or organic solution or dispersion and can be incorporated for this pur pose, for example in cleaning agents, ointment bases, tooth pastes, creams, etc.
The following examples illustrate the invention without limiting it in any way. Parts are always given as parts by weight and the temperatures are in degrees centigrade. V
EXAMPLE 1 OH OH 16.3 parts of 3.4-dichloro-1-phenol are dissolved in 16 parts of methanol; this solution is added dropwise within 3 hours to 250 parts of sulphuric acid at 0-5". 1.5 parts of formaldehyde (as about 40% solution) are then added dropwise within 6 hours at 0-5 whereupon the whole is stirred for 24 hours at 5-10". The reaction product is poured onto ice and the body which then precipitates is isolated, washed with water and dissolved as disodium salt in diluted caustic soda lye. A few resinous side products are removed from this solution by filtration and the latter is acidified with hydrochloric acid. The body which then precipitates as a powder is filtered off, washed with Water until a neutral reaction is obtained and recrystallised twice from benzene. A white crystalline powder with a melting point of 194-196 is so obtained.
CrsHsOzClt:
Calculated C 46.2; H 2.39; Cl 42.0% Found C 46.0; H 2.64; Cl 41.7%
EXAMPLE 2 16.3 parts of 3.4-dichloro-1-phenol are dissolved in 65 parts of glacial. acetic acid. This solution is then slowly added dropwise at 0-5 to parts of 93% sulphuric acid. 1.5 parts of formaldehyde (as about 40% aqueous solution) are added at 0-5 and the whole is stirred for 16 hours at 5-10". The reaction product is poured on to ice and worked up as described in Example 1. A white crystalline powder is obtained which melts at 194-196. 1f 19.8 parts of 3.4.5-trichloro-1-phenol are used instead of 16.3 parts of 3.4-dichloro-l-phenol and the same procedure is followed, after recrystallising from benzene/petroleurn ether, a white body is obtained which melts at 198400".
C13H6O2Cls:
Calculated C1 52.3% Found Cl 52.0%
EXAMPLE 3 ()H (DH 19.7 parts of 3 trifluoromethyl-4-chloro-l-phenol are Pseudo- Staphylo- Staphylo- Esch Salmonella Salmonella Salmonella Ebumena Shzgella moms Com ound coccus coccus a amschot paradysenp mums aims erzchuz colt t 5 S a m an m ententtdts thgphosa mine pyocganes 2.2-dihydroXy-4.5.4.5-tetraehlor0diphenyl methane 6.2 6. 2 333 333 333 333 222 333 500 2.2'-dihydroxy-4.4'-bis-trifluoromethyl-5.5-dichlorodiphenyl methane 3. 1 3. 1 500 222 333 500 222 333 500 2.2-dihydroxy-4.5.6.4.5.G-hexachlor0- diphenyl methane 6. 2 12. 5 333 222 500 500 148 500 X Xzno bactericidal efiect at 500x mol.
dissolved in 200 parts of 93% sulphuric acid. 4.1 parts of a 37% aqueous formaldehyde solution are added dropwise within 5-6 hours to this solution at 5-10". The whole is then stirred for hours during which time the temperature is raised to 20. The reaction mass is poured on to ice, the body which precipitates is isolated and subjected to steam distillation. In this process the unchanged triiluoromethyl-chlorophenol passes over with the steam. The condensation product, thus freed from the starting material is dissolved in 200 parts of water with caustic soda lye as disodium salt. The resinous side products are removed and it is acidified with hydrochloric acid. The condensation product so obtained is still impure. It is recrystallised from benzene therefore whereupon white crystals are obtained. M. P. 181-182".
CrsHsOzClzFe Calculated C 44.4; H 1.99; Cl 17.5% Found C 44.4; H 1.97; Cl 17.5%
Method of comparing the bactericidal activity 0] disinfectants The bactericidal activity of a disinfectant is determined by the minimal concentration which with certainty will kill a standard suspension of test germs under certain conditions. The minimal bactericidal concentration is ascertained with graded concentrations according to the dilution process and is expressed in 10- mol.
Test conditions Sterilised tap water added to 16 hour agar cultures serves as a standard suspension. Its transparency is brought to 85% in the so-called Hellige Bio-Photo-Col apparatus. The standard suspension is mixed with equal amounts of the graded solutions of the disinfectants to be tested (in aqueous solutions). Duration of test: 10 minutes. Temperature: 20 C.
At the end of 10 minutes, two sub-cultures from each reaction mixture are prepared with a glucose broth. The sub-cultures are bred at 37. The development or sterility of the sub-cultures is determined after 48 hours.
What we claim is: 1. A 2.2'-dihydroxydiphenyl methane compound of the formula wherein X represents a member selected from the group consisting of chlorine and the trifluoromethyl group.
2. A 2.2'-dihydroxydiphenyl methane compound having the formula:
References Cited in the file of this patent UNITED STATES PATENTS 2,250,480 Gump July 29, 1941 2,353,725 Gump July 18, 1944 2,544,826 Craig, Jr Mar. 13, 1951 FOREIGN PATENTS 557,097 Great Britain Nov. 4, 1943 OTHER REFERENCES Industrial & Engineering Chemistry," March et 211., vol. 41, pp. 2176-84 (1949).