(IPr)Pd(acac)Cl:  An Easily Synthesized, Efficient, and Versatile Precatalyst for C−N and C−C Bond Formation

Nicolas Marion, Elise C. Ecarnot, Oscar Navarro, Dino Amoroso, Andrew Bell, Steven P. Nolan

The Journal of Organic Chemistry · 2006 · 188 citations · 7 references

Concepts

Abstract

A very straightforward synthesis of (IPr)Pd(acac)Cl from two commercially available starting materials, Pd(acac)2 and IPr.HCl [acac = acetylacetonate; IPr = N,N'-bis(2,6-diisopropylphenyl)imidazol-2-ylidene], has been developed. The resulting complex, (IPr)Pd(acac)Cl (1), has proven to be a highly active PdII precatalyst in the Buchwald-Hartwig and the alpha-ketone arylation reactions. A wide range of substrates has been screened, including unactivated, sterically hindered, and heterocyclic aryl chlorides.

References

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