首页> 外文期刊>RSC Advances >Synthesis of n-alkyl terminal halohydrin esters from acid halides and cyclic ethers or thioethers under solvent- and catalyst-free conditions
【24h】

Synthesis of n-alkyl terminal halohydrin esters from acid halides and cyclic ethers or thioethers under solvent- and catalyst-free conditions

机译:在无溶剂和无催化剂的条件下,由酰基卤与环状醚或硫醚合成正烷基末端卤代醇酯

获取原文
获取原文并翻译 | 示例
           

摘要

An efficient and eco-friendly protocol has been developed for the preparation of n-alkyl terminal halohydrin esters under solvent- and catalyst-free conditions. Ring opening of cyclic ethers by organic acid halides affords the 1,4- and 1,5-halohydrins, OH-protected by different acyl groups. The green reaction conditions, simple work-up procedures, high yields and broad substrate scope of the reaction highlight the positive features of this method.
机译:已经开发了一种有效且环保的方案,用于在无溶剂和无催化剂条件下制备正烷基末端卤代醇酯。通过有机酰基卤将环状醚开环,得到1,4-和1,5-卤代醇,由不同的酰基进行OH保护。绿色的反应条件,简单的后处理程序,高收率和广泛的反应范围突出了该方法的积极特性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号