Reaction of alkylphenols with acetals. II. Reaction of 4methyl-2-tert-butylphenol with dimethoxymethane

Journal Article · Thu Dec 19 23:00:00 EST 1985 · J. Org. Chem. USSR (Engl. Transl.); (United States)

OSTI ID:6263782

Starikova, O F; Gurvich, Y A; Kumok, S T; Styskin, E L

The authors explain how di(hydroxydialkylaryl) derivatives of methane play an important role in the inhibition of oxidation processes in polymers, oils, fuels, and other organic materials. They investigate the reaction of 4-methyl-2-tert-butylphenol with dimethoxymethane, and established that the reaction mass contained 2-methoxymethyl-4-6-tert-butylphenol. The formation and the transformations of 2-methoxymethyl-4-methyl-6-tert-butylphenol do not have a significant effect on the synthesis of di(2-hydroxy-5-methyl-3-tert-butylphenyl) methane from 4-methyl-2-tert-butyl-phenol and dimethoxymethane.

• Research Organization: Sci-Res. Institute of Rubber and Latex Goods, Moscow
• OSTI ID: 6263782
• Journal Information: J. Org. Chem. USSR (Engl. Transl.); (United States), Journal Name: J. Org. Chem. USSR (Engl. Transl.); (United States) Vol. 21:7, PART 2; ISSN JOCYA
• Country of Publication: United States
• Language: English

Related Subjects

02 PETROLEUM
023000* -- Petroleum-- Properties & Composition
ALKANES
ALKOXY RADICALS
AROMATICS
CHEMICAL COMPOSITION
CHEMICAL PROPERTIES
CHEMICAL REACTION KINETICS
CHEMICAL REACTIONS
HYDROCARBONS
HYDROXY COMPOUNDS
KINETICS
METHANE
METHOXY RADICALS
ORGANIC COMPOUNDS
OXIDATION
PETROLEUM PRODUCTS
PHENOLS
RADICALS
REACTION KINETICS