Beckmann rearrangement of oximes catalyzed by cyanuric chloride in ionic liquids.

[摘要]：The Beckmann rearrangement of a variety of ketoximes was carried out in imidazolium-based ionic liqs. in the presence of catalytic amts. of 2,4,6-trichloro[1,3,5]triazine. This mild and green procedure is highly regioselective affording the corresponding N-substituted amides in very good to quant. yields. The ionic liqs. were easily recovered and recycled several times.

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