Chinese Journal of Catalysis ›› 2006, Vol. 27 ›› Issue (12): 1107-1110.

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Asymmetric Hydrogenation of Acetonaphthone Catalyzed by RuCl2[P(C6H5)3]2-(R,R)-DPEN

TAO Ming1*, XIONG Wei1, CHEN Hua2, LI Xianjun2   

  1. 1 Department of Biology and Chemistry, Xichang College, Xichang 615022, Sichuan, China; 2 Institute of Homogeneous Catalysis, College of Chemistry, Sichuan University, Chengdu 610064, Sichuan, China
  • Received:2006-12-25 Online:2006-12-25 Published:2006-12-25

Abstract: A novel ruthenium complex RuCl2[P(C6H5)3]2-(R,R)-DPEN (DPEN=1,2-diphenylethylene-diamine) was synthesized and characterized by 1H and 31P NMR. The ruthenium complex was applied to the asymmetric hydrogenation of acetonaphthone.The effects of reaction temperature, hydrogen pressure, and molar ratio of base to catalyst on the activity and enantioselectivity were investigated in an isopropanol solution of (CH3)3COK. The results showed that the increase in the temperature and pressure accelerated the reaction but slightly decreased the enantioselectivity for (S)-α-naphthylethanol. Under the conditions of acetonaphthone∶(CH3)3COK∶Ru=50000∶450∶1 (molar ratio), 4 MPa, 25 ℃, and 16 h, 83% ee and 100% yield of α-naphthylethanol were achieved.

Key words: ruthenium phosphine complex, chiral diamine, acetonaphthone, asymmetric hydrogenation, α-naphthylethanol, enantioselectivity