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Updated: Jun 12, 2025

A Microwave-Assisted Direct Heteroarylation of Ketones Using Transition Metal Catalysis
Published on: February 16, 2020
Reductively Induced Aryl Transmetalation: An Alternative Catalytically Relevant Ni-Catalyzed Biaryl Coupling
Antonio Romero-Arenas1,2, Mihai V Popescu3, McKenna K Goetz1
1Department of Chemistry, University of Wisconsin-Madison, 1101 University Avenue, Madison, Wisconsin 53706, United States.
None:
Ni-catalyzed cross-electrophile coupling (XEC) reactions have gained prominence for the construction of C-C bonds. Prior studies of XEC routes to biaryls have invoked several different mechanisms for the formation of key Ni(Ar)2 intermediates. Here, we provide evidence for a previously unrecognized pathway involving reductively induced transmetalation between NiI(Ar) and NiII(Ar)X species. Chemical and electrochemical reduction of (tBubpy)NiII(2-tolyl)Br (tBubpy = 4,4'-di-tert-butyl-2,2'-bipyridine) to (tBubpy)NiI(2-tolyl) is shown to initiate rapid transmetalation of the 2-tolyl ligand to a second equivalent of (tBubpy)NiII(2-tolyl)Br, affording (tBubpy)NiII(2-tolyl)2 and (tBubpy)NiIBr as well-defined products. Experimental and computational data show that the NiI-to-NiII transmetalation mechanism is much more favorable than NiII-to-NiII transmetalation. Oxidation of (tBubpy)NiII(2-tolyl)Br results in rapid reductive elimination of 2-tolyl-Br, rather than promoting the analogous oxidatively induced NiII/NiIII transmetalation. The NiII(2-tolyl)2 product of NiI-to-NiII transmetalation is stable at room temperature, while sterically less encumbered NiII(Ar)2 species undergo rapid reductive elimination to afford biaryl and a Ni0 byproduct. The latter species can serve as a source of electrons to promote further transmetalation and biaryl formation. The unhindered complex (tBubpy)NiII(4-CF3-phenyl)Br undergoes biaryl formation in the absence of added reductant; however, kinetic analysis reveals an induction period and autocatalytic time course. Addition of catalytic quantities of a cobaltocene-based reductant eliminates the induction period and accelerates biaryl formation, consistent with the NiI-to-NiII transmetalation pathway. The results of this study provide a new rationale for previously reported results in the literature and introduce an alternative pathway to consider in the development of Ni-catalyzed biaryl coupling reactions.
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