Methods of making compounds having antidegradant and antifatigue efficacy
A method of making antidegradant compounds is disclosed, in which a p-phenylenediamine is reacted with an alpha-hydroxy carbonyl compound to thereby obtain an enediamine, which is reduced to thereby obtain a mixture comprising the antidegradant compound.
1. A method of making an antidegradant compound, the method comprising:
reacting a p-phenylenediamine corresponding to formula IV:
wherein X is selected from the group consisting of alkyl, aryl, alkylaryl groups and hydrogen;
with an alpha-hydroxy carbonyl compound corresponding to formula
wherein R 1 and R 3 are each independently selected from the group consisting of alkyl, aryl, alkylaryl groups and hydrogen,
and wherein R 1 and R 3 may optionally be bridged by a polymethylene group;
to thereby obtain an enediamine; and
reducing the enediamine to thereby obtain a mixture comprising the antidegradant compound according to formula I:
wherein X is each independently selected from the group consisting of alkyl, aryl, alkylaryi groups and hydrogen;
wherein R 1 and R 3 are each independently selected from the group consisting of alkyl, aryl, alkylaryl groups and hydrogen; and
wherein R 1 and R 3 may optionally be bridged by a polymethylene group to form a cycloalkyl.
2. The method of claim 1 , wherein the p-phenylenediamine comprises 4-aminodiphenvlamine.
3. The method of claim 1 , wherein the alpha-hydroxy carbonyl comprises one or more of acetoin acetoin, acetol, and benzoin.
4. The method of claim 1 , wherein the alpha-hydroxy carbonyl comprises acetoin, and wherein the p-phenylenediamine and the alpha-hydroxy carbonyl are reacted in the presence of a solvent and an acid catalyst.
5. The method of claim 4 , wherein the acid catalyst comprises one or more of formic acid, acetic acid, propionic acid, p-toluenesulfonic acid, camphorsulfonic acid, hydrochloric acid, sulfuric acid, phosphoric acid, and a solid-supported acidic resin.
6. The method of claim 4 , wherein the solvent comprises methylisobutylketone and the mixture comprising the antidegradant compound further comprises N-(1,3-Dimethylbutyl)-N′-phenyl-p-phenylenediamine.
7. The method of claim 4 , wherein the solvent comprises acetone and the mixture comprising the antidegradant compound further comprises N-isopropyl-N′-phenyl-p-phenylenediamine.
8. The method of claim 1 , wherein the enediamine is reduced by hydrogenation in the presence of: (a) a solvent, (b) a homogeneous or heterogeneous metal catalyst, and (c) one or more of hydrogen gas, formic acid, or a formic acid salt.
9. The method of claim 1 , wherein the step of reacting the p-phenylenediamine with the alpha-hydroxy carbonyl and the step of reducing the enediamine thereby obtained are carried out in sequence, with optional isolation of the intermediate diimine compound.
10. The method of claim 1 , wherein the step of reacting the p-phenylenediamine with the alpha-hydroxy carbonyl and the step of reducing the enediamine thereby obtained are carried out simultaneously in the same reaction mixture.
11. The method of claim 1 , wherein the antidegradant compound comprises N,N′-(butane-2,3-diyl)bis(N-phenylbenzene-1,4-diamine).