A General Palladium-Catalyzed Amination of Aryl Halides with Ammonia

被引:146
|
作者
Schulz, Thomas [1 ]
Torborg, Christian [1 ]
Enthaler, Stephan [1 ]
Schaeffner, Benjamin [1 ]
Dumrath, Andreas [1 ]
Spannenberg, Anke [1 ]
Neumann, Helfried [1 ]
Boerner, Armin [1 ]
Beller, Matthias [1 ]
机构
[1] Univ Rostock, Leibniz Inst Katalyse eV, D-18059 Rostock, Germany
关键词
amination; anilines; homogeneous catalysis; palladium; phosphanes; CROSS-COUPLING REACTIONS; HIGHLY EFFICIENT CATALYST; BOND-FORMING REACTIONS; LONG-LIVED CATALYSTS; C-N; PRIMARY AMINES; REDUCTIVE CARBONYLATION; HETEROARYL BROMIDES; OXIDATIVE ADDITION; CARBENE CATALYSTS;
D O I
10.1002/chem.200802678
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A study was conducted to demonstrate palladium(Pd)-catalyzed amination of aryl halides with ammonia. The active catalyst was formed in situ from Pd(OAc)2, along with air- and moisture stable phosphines as pre-catalysts. It was found that the productivity of the catalyst system was similar to that of competitive Pd and phosphine systems. It was demonstrated that the novel electron-rich sterically demanding phosphine ligand was unable to be displaced from the palladium by ammonia to a significant extent, which prevented the deactivation of the catalyst by the ligand. It was also demonstrated that the Pd-catalyzed animation worked at ambient pressure. It was observed that the optimized system showed an excellent substrate scope including deactivated, electron-neutral, and activated halides, o-, m- p-substituted substrates, aryl chlorides, and heterocycles.
引用
收藏
页码:4528 / 4533
页数:6
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