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R-3,5-(双三氟甲基)苯乙醇不对称合成工艺
引用本文:蒲国荣,周龙昌,向忠权,孙果宋,韦志明,陈小鹏.R-3,5-(双三氟甲基)苯乙醇不对称合成工艺[J].精细化工,2013(4):468-470.
作者姓名:蒲国荣  周龙昌  向忠权  孙果宋  韦志明  陈小鹏
作者单位:广西大学化学化工学院;广西化工研究院
摘    要:以RuCl2(C10H14)2]2为催化剂、(1S,2R)-(-)-1-氨基-2-茚醇为配体,3,5-双三氟甲基苯乙酮在异丙醇中发生不对称氢化还原反应得到R-3,5-(双三氟甲基)苯乙醇。在反应时间6 h、温度50℃、n(催化剂)∶n(配体)=1∶2.5、底物浓度0.095 7 mol/L的条件下,产品的转化率达99.32%,选择性(ee)达91.2%。用FTIR和1HNMR进行了表征。

关 键 词:3  5-双三氟甲基苯乙酮  不对称合成  R-3  5-(双三氟甲基)苯乙醇  精细化工中间体

Asymmetric Synthesis of R-3,5(Trifluoro-dimethyl) Benzene Ethanol
PU Guo-rong,ZHOU Long-chang,XIANG Zhong-quan,SUN Guo-song,WEI Zhi-ming,CHEN Xiao-peng.Asymmetric Synthesis of R-3,5(Trifluoro-dimethyl) Benzene Ethanol[J].Fine Chemicals,2013(4):468-470.
Authors:PU Guo-rong  ZHOU Long-chang  XIANG Zhong-quan  SUN Guo-song  WEI Zhi-ming  CHEN Xiao-peng
Affiliation:1(1.College of Chemistry and Chemical Engineering,Guangxi University,Nanning 530004,Guangxi,China;2.Guangxi Research Institute of Chemical Industry,Nanning 530001,Guangxi,China)
Abstract:An asymmetric transfer hydrogenation was adopted to synthesize R-3,5-(trifluoro-dimethyl) benzene ethanol from 3,5-bis(trifluoromethyl)acetophenone in isopropyl alcohol by using RuCl2(C10H14)2]2 as catalyst and(1S,2R)-(-)-1-amino-2-indene alcohol as ligands.When the reaction time was 6 h,reaction temperature was 50 ℃,catalyst/ligands molar ratio was 1∶ 2.5,and the substrate concentration was 0.095 7 mol/L,the conversion rate of the product was 99.32%,and selectivity(ee) was 91.2%.The target product was characterized by means of FTIR and 1HNMR.
Keywords:3  5-bis(trifluoromethyl)acetophenone  asymmetric synthesis  R-3  5(trifluoro-dimethyl) benzene ethanol  fine chemical intermediates
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