首页> 外国专利> Substituted 1,1,1-triaryl-2,2,2-trifluoroethanes and processes for their synthesis

Substituted 1,1,1-triaryl-2,2,2-trifluoroethanes and processes for their synthesis

机译:取代的1,1,1-三芳基-2,2,2-三氟乙烷及其合成方法

摘要

Synthetic procedures to tetraalkyls, tetraacids and dianhydrides substituted 1,1,1-triaryl-2,2,2-trifluoroethanes which comprises: (1) 1,1- bis(dialkylaryl)-1-aryl-2,2,2-trifluoroethane, (2) 1, 1-bis(dicarboxyaryl)- 1-aryl-2,2,2-trifluoroethane or (3) cyclic dianhydride or diamine of 1,1- bis(dialkylaryl)-1-aryl-2,2,2- trifluoroethanes. The synthesis of (1) is accomplished by the condensation reaction of an aryltrifluoromethyl ketone with a dialkylaryl compound. The synthesis of (2) is accomplished by oxidation of (1). The synthesis dianhydride of (3) is accomplished by the conversion of (2) to its corresponding cyclic dianhydride. The synthesis of the diamine is accomplished by the similar reaction of an aryltrifluoromethyl ketone with aniline or alkyl substituted or disubstituted anilines. Also, other derivatives of the above are formed by nucleophilic displacement reactions.
机译:四烷基,四酸和二酐取代的1,1,1-三芳基-2,2,2-三氟乙烷的合成程序,包括:(1)1,1-双(二烷基芳基)-1-芳基-2,2,2-三氟乙烷,(2)1、1-双(二烷基芳基)-1-芳基-2,2、1-双(二羧基芳基)-1-芳基-2,2,2-三氟乙烷或(3)环状二酐或二胺, 2-三氟乙烷。 (1)的合成通过芳基三氟甲基酮与二烷基芳基化合物的缩合反应来完成。 (2)的合成通过(1)的氧化来完成。 (3)的合成二酐通过将(2)转化为其相应的环状二酐来完成。二胺的合成通过芳基三氟甲基酮与苯胺或烷基取代或二取代的苯胺的类似反应完成。另外,上述的其他衍生物是通过亲核取代反应形成的。

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