Issue 2, 1997

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

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.

Article information

Article type
Paper

Mendeleev Commun., 1997,7, 61-63

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 and M. E. Vol'pin, Mendeleev Commun., 1997, 7, 61 DOI: 10.1070/MC1997v007n02ABEH000679

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