4.4 Article

Synthesis of diarylmethanes via a Friedel-Crafts benzylation using arenes and benzyl alcohols in the presence of triphenylphosphine ditriflate

期刊

TETRAHEDRON LETTERS
卷 53, 期 38, 页码 5131-5135

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2012.07.051

关键词

Arenes; Benzylation; Electrophilic aromatic substitution; Mitsunobu reaction; Phosphorus

资金

  1. Razi University

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Triphenylphosphine ditriflate (TPPD) was found to be an efficient promoter for the Friedel-Crafts benzylation of arenes with benzyl alcohols in CH2Cl2 at room temperature. The good yields, the 1:1 molar ratio of arene and benzyl alcohol, the benzylation of chlorobenzene as a nonactivated aromatic compound at room temperature, and no by-product formation are the main advantages of this procedure. (C) 2012 Elsevier Ltd. All rights reserved.

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