Xu Hao, Ma Shuang, Xu Yuanqing, Bian Longxiang, Ding Tao, Fang Xiaomin, Zhang Wenkai, Ren Yanrong
Institute of Fine Chemistry and Engineering, Henan Engineering Laboratory of Flame-Retardant and Functional Materials, College of Chemistry and Chemical Engineering, Henan University , Kaifeng 475004, P. R. China.
J Org Chem. 2015 Feb 6;80(3):1789-94. doi: 10.1021/jo502709t. Epub 2015 Jan 26.
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.
通过两种腈与羟胺反应,开发了一种简单高效的铜催化一锅法合成取代1,2,4-三唑的方法。该方法使用简单易得的腈和盐酸羟胺作为起始原料,廉价的醋酸铜作为催化剂,以中等至良好的产率得到相应的1,2,4-三唑衍生物。反应包括羟胺依次对一种腈进行分子间加成以生成偕胺肟,铜催化偕胺肟与另一种腈反应,以及分子内脱水/环化。这一发现为1,2,4-三唑衍生物的合成提供了一种新的有用策略。