Two competing mechanisms for the copper-free Sonogashira cross-coupling reaction
Artikel i vetenskaplig tidskrift, 2008

The mechanism of the copper-free Sonogashira cross-coupling was investigated using a model reaction with differently para-substituted phenylacetylenes and 4-iodobenzotrifluoride as coupling partners and a Pd 2 (dba) 3 -CHCl 3 -AsPh 3 catalyst system in methanol. A carbopalladation mechanism was ruled out through a series of experiments in which the equivalent of a carbopalladation reaction intermediate was synthesized by an alternate route, and its conversion to product was monitored. A Hammett correlation study revealed a possible mechanistic changeover when going from electron-rich to electron-poor alkynes in the model reaction. It is advocated that the reaction mechanism changes from a pathway involving a fast proton transfer from a slowly forming cationic Pd complex to a pathway involving a slow proton transfer from a neutral Pd complex on going from electron-rich to electron-poor alkynes. The amine base is believed to act as a base in both pathways and as a nucleophile promoting the formation of the cationic complex in the reactions involving electron-rich alkynes. This was substantiated by the observation of a primary isotope effect (K Alkyne-H /K Aikyne-D ≈ 2) for the electron-poor alkyne and a pronounced base dependence for the electron-rich one. © 2008 American Chemical Society.

Författare

Thomas Ljungdahl

Chalmers, Kemi- och bioteknik, Organisk kemi

T. Bennur

Chalmers University of Technology

A. Dallas

Chalmers University of Technology

H. Emtenas

Chalmers University of Technology

Jerker Mårtensson

Chalmers, Kemi- och bioteknik, Organisk kemi

Organometallics

0276-7333 (ISSN) 1520-6041 (eISSN)

Vol. 27 11 2490-2498

Ämneskategorier

Kemi

DOI

10.1021/om800251s