氧化锌促进的醛与[Ph3P+CF2H·Br-]的Wittig偕二氟烯基化反应（英文）  

Zn O-Promoted Wittig gem-Difluoroolefination of Aldehydes with [Ph3P+CF2H·Br-]

作　　者：于蛟 林锦鸿[1] 肖吉昌[1] Yu Jiao;Lin Jinhong;Xiao Jichang(Key Laboratory of Organofluorine Chemistry, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai 200032)

机构地区：[1]中国科学院上海有机化学研究所有机氟化学重点实验室中国科学院大学

出　　处：《有机化学》2019年第1期265-269,共5页Chinese Journal of Organic Chemistry

基　　金：Project supported by the National Basic Research Program of China(973 Program,No.2015CB931903);the National Natural Science Foundation of China(Nos.21421002,21472222,21502214,21672242);the Chinese Academy of Sciences(Nos.XDA02020105,XDA02020106),and the Key Research Program of Frontier Sciences(CAS)(No.QYZDJSSW-SLH049)~~

摘　　要：以氧化锌为碱实现了醛与二氟甲基鏻盐[Ph3P+CF2H·Br-]的Wittig偕二氟烯基化反应.虽然鏻盐中二氟甲基上的氢原子具有一定酸性,但是碱不一定就会与其发生中和反应而使鏻盐转化为叶立德.碱也有可能进攻磷原子而产生具有亲核性的二氟甲基物种,从而发生亲核二氟甲基化.以氧化锌为碱可抑制二氟甲基化,有利于Wittig反应;此外,氧化锌及其产生的锌盐都可经简单过滤而除去,方便产物纯化.Wittig gem-difluoroolefination of aldehydes with difluoromethyl phosphonium salt (Ph3P+CF2H·Br-) by using zinc oxide as a base is described. Although the proton in the CF2H group is acidic and a base could easily lead to its deprotonation to form ylide (Ph3P+CF2-), the attack of the base at the positive phosphorus atom may also take place to produce a nucleophilic [HCF2-] equivalent, and then nucleophilic difluoromethylation instead of Wittig reaction would occur. The use of ZnO as the base favored the Wittig reaction and the nucleophilic difluoromethylation was not observed. Furthermore, the excessive ZnO and ZnⅡ salts produced from ZnO could be easily removed by filtration, which may be convenient for the purification process.

关 键 词：WITTIG 偕二氟烯基化 醛 二氟甲基鏻盐 氧化锌 

分 类 号：O621.25[理学—有机化学]