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Dealkylation of Derivatives of 2,6-di-Butylphenol in the Presence of Heteropoly Acids ArticleGenre_short.SHORT_COMMUNICATION

Journal Kinetics and Catalysis
ISSN: 0023-1584 , E-ISSN: 1608-3210
Output data Year: 1986, Volume: 27, Number: 3, Pages: 651-654 Pages count : 4
Tags ACIDS; CATALYSTS
Authors Kulikov S.M. 1 , Kozhevnikov I.V. 1 , Fomina M.N. 1 , Kry'sin A.P. 2
Affiliations
1 Institute of Catalysis, Siberian Branch, Academy of Sciences of the USSR
2 N.N. Vorozhtsov Institute of Organic Chemistry of the Siberian Branch, Academy of Sciences of the USSR

Abstract: The dealkylation of derivatives of 2, 6-di-tert-butylphenol, Ph(tert-butyl)2R (R equals CH3, C2H5, CH2CH2COOCH3), was studied in the presence of heteropoly acids (HPAs) H3PW12O40. HPAs are effective heterogeneous catalysts of the selective elimination of one tertbutyl group from the compounds Ph(tert-butyl)2R. The reaction proceeds in a melt of the substrate at 130-150 degree C. HPAs are substantially more active than the traditional heterogeneous catalysts, such as metal sulfates and cation exchangers.
Cite: Kulikov S.M. , Kozhevnikov I.V. , Fomina M.N. , Kry'sin A.P.
Dealkylation of Derivatives of 2,6-di-Butylphenol in the Presence of Heteropoly Acids
Kinetics and Catalysis. 1986. V.27. N3. P.651-654. WOS Scopus РИНЦ
Original: Куликов С.М. , Кожевников И.В. , Фомина М.Н. , Крысин А.П.
Деалкилирование производных 2,6-ди-третбутилфенола в присутствии гетерополикислот
Кинетика и катализ. 1986. Т.27. №3. С.750-753. РИНЦ ANCAN
Dates:
Submitted: Jul 11, 1985
Published print: May 1, 1986
Identifiers:
Web of science: WOS:A1986F578600020
Scopus: 2-s2.0-0022711624
Elibrary: 23753052
Citing:
DB Citing
Web of science 1
Scopus 1
Elibrary 1