4.4 Article

A convenient and regioselective oxidative bromination of electron-rich aromatic rings using potassium bromide and benzyltriphenylphosphonium peroxymonosulfate under nearly neutral reaction conditions

Journal

TETRAHEDRON LETTERS
Volume 48, Issue 7, Pages 1255-1259

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2006.12.033

Keywords

activated arenes; benzyltriphenylphosphonium peroxymonosulfate; oxidative bromination; potassium bromide

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Regioselective oxidative bromination of electron-rich aromatic rings has been studied using potassium bromide as a bromine source in the presence of benzyltriphenylphosphonium peroxymonosulfate as oxidant under nearly neutral reaction conditions. In most cases we obtained monobrominated derivatives regioselectively and in good to high yields without the aid of strong acids. (c) 2006 Elsevier Ltd. All rights reserved.

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