Synthesis of α-trifluoromethyl ethanone oximes via the three-component reaction of aryl-substituted ethylenes, tert-butyl nitrite, and the Langlois reagent

Literature Information

Publication Date 2019-10-01
DOI 10.1039/C9QO00940J
Impact Factor 5.281
Authors

Kui Lu, Quan Li, Liangshuo Ji, Erbing Hua, Yujie Dai, Xia Zhao


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Abstract

A mild and simple protocol for the synthesis of α-trifluoromethylated ethanone oximes from aryl-substituted ethylenes, tert-butyl nitrite, and the Langlois reagent was developed under transition metal-free conditions. In this three-component reaction, tert-butyl nitrite was employed not only as the oxidant but also as the oxime source. A range of α-trifluoromethylated ethanone oximes were obtained, indicating the wide substrate scope of the reaction.

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Organic Chemistry Frontiers
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