Copper-Catalyzed One-Pot Synthesis of 1,2,4-Triazoles from Nitriles and Hydroxylamine

A simple and efficient copper-catalyzed one-pot synthesis of substituted 1,2,4-triazoles through reactions of two nitriles with hydroxylamine has been developed. The protocol uses simple and readily available nitriles and hydroxylamine hydrochloride as the starting materials and inexpensive Cu­(OAc)...

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Veröffentlicht in:Journal of organic chemistry 2015-02, Vol.80 (3), p.1789-1794
Hauptverfasser: Xu, Hao, Ma, Shuang, Xu, Yuanqing, Bian, Longxiang, Ding, Tao, Fang, Xiaomin, Zhang, Wenkai, Ren, Yanrong
Format: Artikel
Sprache:eng
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Zusammenfassung:A simple and efficient copper-catalyzed one-pot synthesis of substituted 1,2,4-triazoles through reactions of two nitriles with hydroxylamine has been developed. The protocol uses simple and readily available nitriles and hydroxylamine hydrochloride as the starting materials and inexpensive Cu­(OAc)2 as the catalyst, and the corresponding 1,2,4-triazole derivatives are obtained in moderate to good yields. The reactions include sequential intermolecular addition of hydroxylamine to one nitrile to provide amidoxime, copper-catalyzed treatment of the amidoxime with another nitrile, and intramolecular dehydration/cyclization. This finding provides a new and useful strategy for synthesis of 1,2,4-triazole derivatives.
ISSN:0022-3263
1520-6904
DOI:10.1021/jo502709t