4.4 Article

Novel and highly efficient one pot protocol for the synthesis of diversely functionalized triarylmethanes

Journal

TETRAHEDRON LETTERS
Volume 56, Issue 6, Pages 766-771

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2014.11.139

Keywords

Triarylmethanes; Friedel-Crafts reaction; Oxidation; BF3 center dot OEt2; Lewis acid

Funding

  1. CSIR
  2. CSIR, New Delhi [CSC-0301]

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An efficient, convenient, and novel one pot approach is described for the synthesis of triarylmethanes by in situ oxidation of benzylalcohols followed by the Friedel-Crafts alkylation of di/trimethoxybenzenes in the presence of BF3 center dot OEt2. The generality of the present method is strengthened by screening a variety of aromatic, aliphatic, and heteroaromatic alcohols with methoxy arenes. Shorter reaction time, mild reaction condition, good yields, and wide scope of substrates are the significant features of this protocol. (C) 2014 Elsevier Ltd. All rights reserved.

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