Interaction of functionally-substituted 4-alkyl-2, 6-di-tert-butylphenols with hydrohalic acids

AE Prosenko, AA Skorobogatov, OI Dyubchenko…

Index: Prosenko; Skorobogatov; Dyubchenko; Pinko; Kandalintseva; Shakirov; Pokrovsky Russian Chemical Bulletin, 2007 , vol. 56, # 6 p. 1119 - 1124

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Citation Number: 2

Abstract

Abstract 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- ...

~59%

~45%

~82%

~43%

~76%

~77%

~91%

~90%

~93%

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