Bactericidic and fungicidic chloromethylisopropylphenols

Abstract

Chloromethylisopropylphenois, namely 4-chloro-3-methyl-2-isopropyl phenol, 4-chloro-3-methyl-5-isopropyl phenol and their 6,6'-methylene and 2,2'-methylene bis derivatives, effective as a bactericide and fungicide, especially against staphylococcus, pneumococcus and tricoccus. They are effective in doses as low as 5 ppm, are stable, substantially odor-free and can be readily prepared by conventional chemical reactions to obtain a substantially nontoxic white product.

Description

FIELD OF THE INVENTION

Our invention relates to bactericidal and fungicidal chloromethylisopropylphenols, to a method of making same and to treatment using these compounds.

OBJECT OF THE INVENTION

The principal object of our invention is to provide efficient and economical agents for the treatment of infectious diseases.

Another object of our invention is to provide stable, odorless and nontoxic agents against staphylococcus, pneumococcus, trichomonas and various fungus diseases.

DESCRIPTION OF THE INVENTION

We have found that the following chloromethylisopropylphenols have valuable properties as therapeutic agents, especially for combatting staphylococcus, pneumococcus, trichomonas and various fungus diseases:

4-chloro-3-methyl-2-isopropyl-phenol (I); 4-chloro-3-methyl-5-isopropyl-phenol (II); 6,6'-methylene-bis (4-chloro-3-methyl-2-isopropyl)-phenol (III); and 2,2'-methylene-bis(4-chloro-3-methyl-5-isopropyl)phenol (IV).

these compounds have the following valuable properties:

The are characterized by surprisingly high bactericide and fungicide activity in comparison with similar products;

The are very stable and do not decompose easily; and

They can be obtained in very pure condition, without any toxic byproduct or trace compound present, by simple conventional processes.

They can be characterized as follows:

Appearance and Odor;

I, II and III: white crystals having a light odor; IV: white grains, substantially odor-free.

Chemical Nature:

I and II: 4-chloro-3-methyl-2-isopropyl-phenol and 4-chloro-3-methyl-5-isopropyl-phenol. ______________________________________Empirical Formula C.sub.10 H.sub.13 ClOStructural Formula: ##STR1## ##STR2##Molecular Weight: : 184,66Elemental Composition in percent (by weight)calculated C 65.04 H 7.09 Cl 19.19found (I) 65.27 6.93 18.90(II) 65.10 7.15 19.45______________________________________ Iii and IV: 6,6' methylen-bis(4-chloro-3-methyl-2-isopropyl; and 2,2' methylene-bis(4-chloro-3-methyl-5-isopropyl) phenol. ______________________________________Empirical Formula: C.sub.21 H.sub.26 Cl.sub.2 O.sub.2Structural Formula: ##STR3## ##STR4##Molecular Weight: 381.34Elemental Composition in percent (by weight):calculated C 66.14 H 6.87 Cl 18.59found (III) 66.39 6.82 18.83(IV) 66.12 6.99 18.51______________________________________ Melting Points: I=52.degree. C; II=43.5.degree. C; III=130.degree. C; and IV=175.degree. C

Nuclear Magnetic Resonance Spectrums:

The lines in nuclear magnetic resonance spectrums correspond well with the proposed formulas as far as position (location) and intensity are concerned. Their positions are listed in the following Table:

______________________________________ Type of MultipletPhenol Solvent Protons Multiplet Center______________________________________ ##STR5## CH(CH.sub.3).sub.2 doublet 1.36 CH.sub.3 singulet 2.35 CH(CH.sub.3).sub.2 septuplet 3.38 H aromatic quadruplet 6.84 OH signal presentII ##STR6## CH(CH.sub.3).sub.2 doublet 1.17 CH.sub.3 singulet 2.25 CH(CH.sub.3).sub.2 septuplet 3.31 H aromatic singulet 6.72 OH signal presentIII CCl.sub.4 CH(CH.sub.3).sub.2 doublet 1.32 CH.sub.3 singulet 2.31 CH(CH.sub.3).sub.2 septuplet 3.35 CH.sub.2 singulet 3.70 OH singulet 5.6 H aromatic singulet 7IV CDCL.sub.3 CH(CH.sub.3).sub.2 doublet 1.14 CH.sub.3 singulet 2.40 CH(CH.sub.3).sub.2 septuplet 3.38 CH.sub.2 singulet 4.05 H aromatic singulet 6.63 OH singulet 6.63______________________________________

EXAMPLE I

4-chloro-3-methyl-2-isopropyl-phenol and 4-chloro-3-methyl-5-isopropyl-phenol

135 g sulfurylchloride is added slowly to 150 g phenolic base and a reaction takes place at 60.degree. - 90.degree. C. When the addition is terminated, the reaction mixture is neutralized with normal caustic potash. The resulting phenolic phase is decanted and washed with distilled water.

The chlorination in this manner of 3-methyl-2-isopropyl-phenol gives 170 g raw product containing approximately 50% by weight of compound I. This raw product can be recovered by distillation and recrystallized in petroleum ether to yield 60 g pure compound I with a melting point of 52.degree. C. The yield is 32%.

The chlorination of 3-methyl-5-isopropyl-phenol gives 175 g raw product containing approximately 75% by weight of compound II. This raw product is distilled and recrystallized in petroleum ether. The yield is 80 g of II, which is pure and melts at 43.5.degree. C. The yield is 43%.

EXAMPLE II

6,6'-methylene-bis(4-chloro-4-methyl-2-isopropyl)phenol and 2,2'-methylene-bis(4-chloro-3-methyl-2-isopropyl)phenol.

6.6 g caustic potash is added to 184.6 g of compound I, then 314 g isopropyl alcohol; this mixture is heated to 45.degree. C and 42 g 36%-formaldehyde is added. This mixture is maintained at 45.degree. C and agitated for six hours and then cooled to ambient temperature. The potash is neutralized with 20 g diluted hydrochloric acid and 550 g petroleum ether is added.

The resulting water phase is decanted and the solvent is completely evaporated. The residue is a brown sticke mass, 190 g, which is redissolved in petroleum ether. Recrystallization gives 75 g pure compound III, which is a satisfactory yield of 38%.

Compound IV can be prepared in the same manner. The yield is 30%.

The compounds I - IV have excellent therapeutic properties. They can be used for treating infections caused by staphylococcus, pneumococcus and trichomonas and mycosis, e.g. candidosis. They are administered as water solutions by local or topical application, having very low concentrations of the compounds (approximately 5 ppm) and are then most effective and, in addition, are totally nontoxic.

The compounds can be generally described by the formula: ##STR7## where the members R.sub.1, R.sub.2 and R.sub.3 are each hydrogen, isopropyl or methylenechloromethylisopropylphenol and at least one of the members R.sub.1, R.sub.2 or R.sub.3 is isopropyl.

Claims

1. 6,6'-methylene-bis(4-chloro-3-methyl-2-isopropil)-phenol.

2. 2,2'-methylene-bis(4-chloro-3-methyl-5-isopropyl)-phenol.