95970-35-7Relevant academic research and scientific papers
Interaction of functionally-substituted 4-alkyl-2,6-di-tert-butylphenols with hydrohalic acids
Prosenko,Skorobogatov,Dyubchenko,Pinko,Kandalintseva,Shakirov,Pokrovsky
, p. 1119 - 1124 (2008/09/18)
Reactions of 4-alkyl-2,6-di-tert-butylphenols containing OH, SH, COOH, and COOMe groups in their para substituents with hydrogen chloride and hydrohalic acids were studied. One-step transformations of 2,6-di-tert-butyl-4-(ω- hydroxyalkyl)phenols to the corresponding 4-(ω-halogenoalkyl)phenols, as well as of 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionic acid and its esters to phloretic acid were proposed. 4-(3-Mercaptopropyl)phenol upon heating with conc. HBr undergoes condensation to 3-(4-hydroxyphenyl)propyl 4-(3-mercaptopropyl)phenyl sulfide as the main product.
THERMAL DE-TERT-BUTYLATION OF 2,6-DI-TERT-BUTYLPHENOL AND ITS DERIVATIVES
Kun, O. B.,Nogina, N. I.,Ostashevskaya, L. A.,Egorov, E. M.,Kuzubova, L. I.,Krysin, A. P.
, p. 2375 - 2378 (2007/10/02)
When heated at 270-300 deg C, 2,6-di-tert-butylphenol and its 4-alkyl, 4-(chloroalkyl), 4-(hydroxyalkyl), and 4-(methoxycarbonyl) derivatives give the corresponding unsubstituted and 4-substituted 2-tert-butylphenols.Removal of the two tert-butyl groups from 2,6-di-tert-butylphenol is observed at temperatures above 300 deg C.
