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

Journal Article · Fri Dec 20 00:00:00 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), Vol. 21:7, PART 2; Other Information: Translated from Zhurnal Organicheskoi Khimii, Vol. 21, No. 7, pp. 1496-1501, July, 1985
• Country of Publication: United States
• Language: English

Related Subjects

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