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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 1997 Volume 7, Issue 2, Pages 61–63 (Mi mendc4783)

This article is cited in 9 papers

Alkylation of deactivated arenes by alkanes in the presence of aprotic organic superacid CBr4·2AlBr3

A. V. Orlinkov, I. S. Akhrem, L. V. Afanas'eva, E. I. Mysov, M. E. Vol'pin

A.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences, Moscow, Russian Federation

Abstract: Deactivated arenes (di- and tri-halobenzenes, acetophenone, benzophenone and methylbenzoate) have been shown to be alkylated by alkanes and cycloalkanes (propane, n-butane, cyclopentane) in the presence of superacid CBr4·2AlBr3 in the range –40 to 0 °C; in some cases selective and effective mono- or di-alkylation can be achieved.

Language: English

DOI: 10.1070/MC1997v007n02ABEH000679



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