Direct, catalytic hydroaminoalkylation of unactivated olefins with N-alkyl arylamines

作者：Herzon Seth B; Hartwig John F^*

来源：Journal of the American Chemical Society, 2007, 129(21): 6690-+.

DOI：10.1021/ja0718366

A tantalum-catalyzed addition of N-alkyl arylamine alpha-C-H bonds across olefins is reported. These reactions occur with mono- and 2,2-disubstituted olefins to form the branched insertion products in high yield and regioselectivity. The reactions encompass additions of the alpha-C-H bonds of cyclic and acyclic amines, as well as intramolecular additions. NMR studies indicate that the starting homoleptic, Ta(NMe2)(5) precatalyst converts to bis- and tris(N-methylanilide) complexes (among others) in solution. Deuterium-labeling studies suggest that reversible ortho-metalation of the arene substituent occurs under the reaction conditions. However, several experiments imply that this ortho-metalation does not lie on the reaction pathway. Instead, these complexes are proposed to eliminate amine to form N-aryl imine complexes, which insert olefins into the Ta-C bond and undergo protonolysis to regenerate the active catalyst and eliminate the addition product.

• 出版日期2007-5-30