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Ru-(S)-BINAP/γ-Al2O3催化剂上苯乙酮及其衍生物的多相不对称加氢反应

Heterogeneous Asymmetric Hydrogenation of Acetophenone and Its Derivatives over Ru-(S)-BINAP/γ-Al2O3

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【作者】 黄艳轶马红霞熊伟陈华李贤均

【Author】 HUANG Yanyi1, MA Hongxia1, XIONG Wei 1,2, CHEN Hua1, LI Xianjun 1*(1 Institute of Homogeneous Catalysis, College of Chemistry, Sichuan University, Chengdu 610064, Sichuan, China; 2 Department of Chemistry, Xichang College, Xichang 615022, Sichuan, China)

【机构】 四川大学化学学院有机金属络合催化研究所四川大学化学学院有机金属络合催化研究所 四川成都610064四川成都610064四川成都610064西昌学院化学系四川西昌615022四川成都610064

【摘要】 在温和条件下制备了Ru (S) BINAP/γ Al2 O3 催化剂 ,考察了其催化苯乙酮及其衍生物不对称加氢的活性 .在KOH 异丙醇溶液中 ,在c(KOH) =0 0 4mol/L ,氢气压力 5MPa和 10℃条件下 ,(1S ,2S) DPEN手性修饰剂修饰的Ru (S) BINAP/γ Al2 O3 催化剂具有较高的活性和对映选择性 ,反应 2 8h后苯乙酮的转化率可达 10 0 % ,(R) 苯乙醇的ee值可达 75 0 % .

【Abstract】 The enantioselective hydrogenation of acetophenone and its derivatives over Ru-(S)-BINAP/γ-Al 2O 3 catalyst using (1S,2S)-1,2-diphenylethylenediamine ((1S,2S)-DPEN) as chiral modifier was investigated. The effect of DPEN, concentration of KOH in i-PrOH, temperature, hydrogen pressure and reaction time on the asymmetric hydrogenation of acetophenone was discussed. (1S,2S)-DPEN played a key role in the chiral inducement and accelerated the asymmetric hydrogenation of acetophenone and its derivatives. Under the optimum conditions of concentration of KOH in i-PrOH of 0 04 mol/L, H 2 pressure of 5 0 MPa, temperature of 10 ℃ and reaction time of 28 h, the conversion of acetophenone and ee value of (R)-phenylethanol reached 100% and 75 0%, respectively. The Ru-(S)-BINAP/γ-Al 2O 3 catalyst could also be used in the asymmetric hydrogenation of acetophenone derivatives such as 2′-fluoroacetophenone, 2′-chloroacetophenone and 2′-bromoacetophenone, but ee values of their products were lower than that of α-phenylethanol produced from acetophenone hydrogenation.

  • 【文献出处】 催化学报 ,Chinese Journal of Catalysis , 编辑部邮箱 ,2004年12期
  • 【分类号】O643
  • 【被引频次】26
  • 【下载频次】372
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