首页> 外国专利> Stereoselective preparation of Z-1,2-diarylallyl chlorides and the conversion thereof into azolylmethyloxiranes, and novel intermediates

Stereoselective preparation of Z-1,2-diarylallyl chlorides and the conversion thereof into azolylmethyloxiranes, and novel intermediates

机译:Z-1,2-二芳基烯丙基氯化物的立体选择性制备及其向偶氮甲基甲基环氧乙烷的转化以及新型中间体

摘要

The preparation of Z-1,2-diarylallyl chlorides of the general formula I ##STR1## in which R.sup.1 and R.sup.2, independently of one another, are hydrogen, halogen, alkyl, haloalkyl, alkoxy, haloalkoxy or a substituted aromatic radical, and n and m are 1, 2 or 3, by dehydrating chlorohydrins of the formula II ##STR2## in which the radicals are as defined above, at up to 50° C. in an inert ether or carboxylic acid ester as solvent and in the presence of a carboxylic anhydride and an organic or inorganic acid, the conversion thereof into azolylmethyloxiranes, and novel intermediates are described.
机译:通式I的Z-1,2-二芳基烯丙基氯化物的制备,其中R 1和R 2彼此独立地是氢,卤素,烷基,卤代烷基,烷氧基通过在惰性条件下在最高50°C下使式II的氯代醇脱水,其中n和m为1、2或3,其中卤代烷氧基或取代的芳族基团的n和m为1、2或3。描述了作为溶剂的醚或羧酸酯,并在羧酸酐和有机或无机酸的存在下,将其转化为偶氮基甲基氧杂环戊烷,以及新型中间体。

著录项

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

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