发明授权
US08729303B2 2,2′,6,6′-tetrasubstituted aminophosphine ligand and its synthesis method
有权
2,2',6,6'-四取代氨基膦配体及其合成方法
- 专利标题: 2,2′,6,6′-tetrasubstituted aminophosphine ligand and its synthesis method
- 专利标题(中): 2,2',6,6'-四取代氨基膦配体及其合成方法
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申请号: US12377000申请日: 2007-08-10
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公开(公告)号: US08729303B2公开(公告)日: 2014-05-20
- 发明人: Wanbin Zhang , Fang Xie , Fang Fang
- 申请人: Wanbin Zhang , Fang Xie , Fang Fang
- 申请人地址: CN Shanghai
- 专利权人: Shanghai Jiaotong University
- 当前专利权人: Shanghai Jiaotong University
- 当前专利权人地址: CN Shanghai
- 代理机构: Westerman, Hattori, Daniels & Adrian, LLP
- 优先权: CN200610029881 20060810
- 国际申请: PCT/CN2007/002407 WO 20070810
- 国际公布: WO2008/019598 WO 20080221
- 主分类号: C07F9/02
- IPC分类号: C07F9/02
摘要:
The present invention relates to a 2,2′,6,6′-tetrasubstituted aminophosphine ligand and its synthesis method. The structure of the ligand is shown as below. Its synthesis method comprises: Step (1) coupling 2,6-dinitrochlorobenzene as the starting material to obtain 2,2′,6,6′-tetranitrobiphenyl; Step (2): hydrogenating the 2,2′,6,6′-tetranitrobiphenyl with Pd/C to obtain 2,2′,6,6′-tetraminobiphenyl; Step (3): reacting the 2,2′,6,6′-tetraminobiphenyl with a phosphine halide to obtain the 2,2′,6,6′-tetrasubstituted aminophosphine ligand. The ligand of the present invention is an achiral compound, and its preparation method is simple. The ligand can be converted to a chiral bimetallic catalyst with single configuration eventually through introduction of external chirality. Moreover, the ligand can be used in various asymmetric reaction catalyzed by metals with high reactivity and stereoselectivity.
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