Chinese Journal of Organic Chemistry >
Efficient Synthesis of β-Amino Alcohols Promoted by Triphenylbismuth Bisperfluorooctanesulfonates
Received date: 2015-10-29
Revised date: 2016-01-21
Online published: 2016-01-29
Supported by
Projected support by the National Natural Science Foundation of China (No. 21373003), the Natural Science Foundation of Hunan Province (No. 14JJ7027), and the Key Project of Hunan Province Education Department (No. 15A041).
In this paper, a novel air-stable triphenylbismuth bisperfluorooctanesulfonate was synthesized by treatment of moisture-sensitive triphenylbismuth dichloride with silver bisperfluorooctanesulfonate in anhydrous CH2Cl2 at room temperature. Its catalytic assessment results show that the reactions of arylamine and epoxide proceed efficiently in the presence of triphenylbismuth bisperfluorooctanesulfonates 1(5.0 mol%) under solvent-free condition, affording β-amino alcohols in good to excellent yields. The yields of desired products do not reduce obviously after recycling for 4 times of catalyst 1. Hence, a convenient and efficient method for preparation of β-amino alcohols is provided.
Tan Nianyuan , Wang Penghui , Xu Xinhua , Gao Qingsong , Au Chaktong , Qiu Renhua . Efficient Synthesis of β-Amino Alcohols Promoted by Triphenylbismuth Bisperfluorooctanesulfonates[J]. Chinese Journal of Organic Chemistry, 2016 , 36(5) : 1094 -1098 . DOI: 10.6023/cjoc201510035
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