首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >A mild and efficient method for one-step alpha-haloacetalization of acetophenones using 1,3-dihalo-5,5-dimethylhydantoin in ethylene glycol
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A mild and efficient method for one-step alpha-haloacetalization of acetophenones using 1,3-dihalo-5,5-dimethylhydantoin in ethylene glycol

机译:一种简单有效的方法,用于乙二醇中的1,3-二卤代-5,5-二甲基乙内酰脲,一步一步进行乙酰苯的α-卤代缩醛化

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摘要

A mild and efficient method that could directly prepare alpha-haloacetal acetophenones from various acetophenones with 1,3-dihalo-5,5-dimethylhydantoin (DBDMH/DCDMH) and ethylene glycol in good yields without catalysts was reported. The effects of solvents, 1,3-dihalo-5,5-dimethylhydantoin, and reaction temperature were investigated. Under the optimal condition, most of a-haloacetal acetophenones were obtained in 65-97% yields. (C) 2015 Elsevier Ltd. All rights reserved.
机译:报道了一种温和而有效的方法,该方法无需使用催化剂即可从各种苯乙酮与1,3-二卤代5,5-二甲基乙内酰脲(DBDMH / DCDMH)和乙二醇直接直接从各种苯乙酮制备α-卤代乙醛苯乙酮。研究了溶剂,1,3-二卤代-5,5-二甲基乙内酰脲和反应温度的影响。在最佳条件下,大多数α-卤缩醛苯乙酮的产率为65-97%。 (C)2015 Elsevier Ltd.保留所有权利。

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