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Transalkylation of Phenols over Heteropoly Acids Full article

Journal Reaction Kinetics and Catalysis Letters
ISSN: 0133-1736 , E-ISSN: 1588-2837
Output data Year: 1991, Volume: 45, Number: 2, Pages: 257-263 Pages count : 7 DOI: 10.1007/BF02070436
Tags Physical Chemistry; Phenol; Toluene; Catalysis; Effective Catalyst
Authors Kozhevnikov I.V. 1 , Kulikov S.M. 1 , Timofeeva M.N. 1 , Krysin A.P. 1 , Titova T.F. 1
Affiliations
1 Institute of Catalysis, Novosibirsk 630090, USSR

Abstract: Transalkylation of 2,6-di-tert-butyl-4-R-phenols over solid heteropoly acids (H3PW12O40, H4SiW12O40, H3PW12O40/SiO2, H4SiW12O40/SiO2) in the presence of toluene or o-xylene as acceptors of a tert-butyl group at 100–140 °C produces 4-R-phenols with 92–98% yield (R = H, alkyl, aryl, etc.). HPAs are effective catalysts for the transalkylation of p-cresol and 2, 6-ditert-butyl-4-methylphenol.
Cite: Kozhevnikov I.V. , Kulikov S.M. , Timofeeva M.N. , Krysin A.P. , Titova T.F.
Transalkylation of Phenols over Heteropoly Acids
Reaction Kinetics and Catalysis Letters. 1991. V.45. N2. P.257-263. DOI: 10.1007/BF02070436 WOS Scopus РИНЦ ANCAN OpenAlex
Dates:
Submitted: Apr 10, 1991
Accepted: May 9, 1991
Published print: Nov 1, 1991
Identifiers:
Web of science: WOS:A1991GV89200014
Scopus: 2-s2.0-0026261498
Elibrary: 31078500
Chemical Abstracts: 1992:447633
Chemical Abstracts (print): 117:47633
OpenAlex: W2015362016
Citing:
DB Citing
Web of science 14
Scopus 12
Elibrary 12
OpenAlex 14
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