Synthesis 2003(17): 2629-2631  
DOI: 10.1055/s-2003-42431
SHORTPAPER
© Georg Thieme Verlag Stuttgart · New York

A Selective and Mild Oxidation of Primary Amines to Nitriles with Trichloroisocyanuric Acid

Fen-Er Chen*, Yun-Yan Kuang, Hui-Fang Dai, Liang Lu, Ming Huo
Department of Chemistry, Fudan University, Shanghai, 200433, P. R. China
Fax: +86(21)65642021; e-Mail: rfchen@fudan.edu.cn;
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Publikationsverlauf

Received 4 August 2003
Publikationsdatum:
14. Oktober 2003 (online)

Abstract

An efficient and highly selective method for the oxidative conversion of primary amines to the corresponding nitriles using trichloroisocyanuric acid in the presence of catalytic TEMPO under mild reaction conditions is described. Other functional groups such as C,C-double bonds, benzyloxy etc. were found to be unaffected under the reaction conditions. This procedure provides a new entry to the synthesis of various aliphatic, aromatic and heterocyclic nitriles in excellent yield.