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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
【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.
【Key words】 acetophenone; ruthenium; chiral ligand; chiral modifier; asymmetric hydrogenation; phenethyl alcohol;
- 【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