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一种合成多氟联苯类化合物的新方法
引用本文:计燕萍,杨芸,高广春.一种合成多氟联苯类化合物的新方法[J].合成化学,2016,24(3):259-262.
作者姓名:计燕萍  杨芸  高广春
作者单位:嘉兴学院 医学院药学系,浙江 嘉兴 314001
摘    要:以CuI为催化剂,芳胺与多氟苯经重氮化/偶联一锅反应生成了6个多氟取代的联苯类化合物(3a~3f),收率56%~82%,其结构经1H NMR, 19F NMR和EI-MS确证。在最佳反应条件[1a 2 mmol, 20%CuI为催化剂,150%四丁基碘化铵为碘化试剂,V(DMSO):V(MeCN)=1 : 1为溶剂,于130 ℃反应4 h]下,3a收率75%。

关 键 词:偶联反应  重氮化反应  多氟联苯  合成  
收稿时间:2015-12-25

A New Method for Synthesis of Multiple Fluorine Substituted Biaryl Compounds
JI Yan-ping,YANG Yun,GAO Guang-chun.A New Method for Synthesis of Multiple Fluorine Substituted Biaryl Compounds[J].Chinese Journal of Synthetic Chemistry,2016,24(3):259-262.
Authors:JI Yan-ping  YANG Yun  GAO Guang-chun
Institution:Pharmacy Department, Medical College,  Jiaxing University, Jiaxing 314000, China
Abstract:A new one-pot synthetic method to prepare multiple fluorine substituted biaryl compounds (3a~3f) by diazotization/cross-coupling of aromatic anilines with polyfluoroarenes had been devel-oped.The yields were 56%~82%.The structures were confirmed by 1 H NMR, 19 F NMR and EI-MS.Under the optimized conditions1a 2 mmol, 20%CuI as the catalyst,150%Bu4 NI as the iodide reagent, V( DMSO) ∶V( MeCN)=1 ∶1 as the solvent, at 130 ℃for 4 h] , the yield of 3a was 75%.
Keywords:coupling reaction  diazotization  fluorobiphenyl  synthesis
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