The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.
The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.
Patent No.:
Date of Patent:
Mar. 23, 1976
Filed:
Oct. 28, 1970
Felix Borisovich Gershanov, Sterlitamak, SU;
Alexandr Grigorievich Liakumovich, Sterlitamak, SU;
Jury Ivanovich Michurov, Sterlitamak, SU;
Boris Izrailevich Pantukh, Sterlitamak, SU;
Grigory Iosifovich Rutman, Sterlitamak, SU;
Valerian Mikhailovich Sobolev, Moscow, SU;
Alexandr Afroimovich Grinberg, Moscow, SU;
Yakov Abramovich Gurvich, Moscow, SU;
Nina Vasilievna Zakharova, Sterlitamak, SU;
Almira Mudarisovna Nafikova, Sterlitamak, SU;
Other;
Abstract
A method of producing 2,6-dialkyl- and 2,6-diaralkyl-substituted derivatives of p-cresol of the general formula ##SPC1## Wherein R signifies an alkyl group having from 4 to 12 carbon atoms or ##SPC2## Comprising subjecting phenol to alkylation with olefines having from 4 to 12 carbon atoms or with styrene at a temperature of 50.degree.-150.degree.C in the presence of a catalyst, namely, aluminum, taken in an amount of 0.1-5 wt.% of phenol. 2,6-Dialkyl phenol or 2,6-diaralkyl phenol resulting after from the alkylation is treated with a mixture of formaldehyde and dimethylamine or with a product of their interaction having the formula ##EQU1## at a temperature of 20.degree.-100.degree.C with subsequent catalytic hydrogenolysis of N,N-dimethyl(3,5-dialkyl-4-hydroxybenzyl)/amine or N,N-dimethyl(3,5-diaralkyl-4-hydroxybenzyl/amine at a temperature of 80.degree.-200.degree.C., molar ratio of hydrogen to the product being treated of 1-5:1 and space velocity of 0.1-2 hour.sup..sup.-1. The products produced by said method feature a high degree of purity, and they can be employed as effective inhibitors of thermooxidation degradation of polymers and hydrocarbon fuels, and also as intermediates for producing p-cresol, and 2-alkyl- and 2-aralkyl-substituted derivatives of p-cresol.