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γ-Hydroxypropylation of 2,6-Dialkyl(aryl)phenols with Allyl Alcohol and Its Derivatives Science article

Общее Language: Английский, Genre: Full article,
Status: Published, Source type: Translated
Journal Russian Journal of General Chemistry
ISSN: 1070-3632 , E-ISSN: 1608-3350
Output data Year: 2010, Volume: 80, Number: 11, Pages: 2290-2297 Pages count : 8 DOI: 10.1134/S1070363210110101
Authors Krysin A.P. 1 , Khalikova N.U. 1 , Khlebnikova T.B. 2 , Nogina N.I. 1 , Mamatyuk V.I. 1
Affiliations
1 Vorozhtzov Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Science
2 Boreskov Institute of Catalysis SB RAS

Abstract: The composition of the products of the reaction of 2,6-disubstituted phenols with allyl alcohol and its derivatives in an alkaline medium was investigated, the conditions for carrying out the reaction with the predominant formation of 4-(3-hydroxypropyl)-2,6-dialkyl(aryl)phenols were found, and its mechanism was suggested. The reaction was examined on an industrial scale. An important result is the practical demonstration of alkaline catalysis performed under homogeneous conditions with participation of phenols, when the used alkaline catalyst is recovered in the process without the formation of waste waters.
Cite: Krysin A.P. , Khalikova N.U. , Khlebnikova T.B. , Nogina N.I. , Mamatyuk V.I.
γ-Hydroxypropylation of 2,6-Dialkyl(aryl)phenols with Allyl Alcohol and Its Derivatives
Russian Journal of General Chemistry. 2010. V.80. N11. P.2290-2297. DOI: 10.1134/S1070363210110101 WOS Scopus РИНЦ AN: 2010:1623221 CAN: 154:258923
article_link_type.translated_to_original: Крысин А.П. , Халикова Н.У. , Хлебникова Т.Б. , Ногина Н.И. , Маматюк В.И.
Гамма-гидроксипропилирование 2, 6-диалкил (арил) фенолов аллиловым спиртом и его производными
Журнал общей химии. 2010. Т.80. №11. С.1826-1833. РИНЦ
Dates:
Submitted: Jan 21, 2010
Published print: Nov 1, 2010
Published online: Dec 25, 2010
Identifiers:
Chemical Abstracts 2010:1623221
Chemical Abstracts (print) 154:258923
Web of science WOS:000286663100010
Scopus 2-s2.0-79251474970
Rinz 16713822
Links:
  • Web of science - publication.cite_link
  • Scopus - publication.cite_link
  • Rinz - publication.cite_link
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