Clean and fast cross-coupling of aryl halides in one-pot

Beilstein J Org Chem. 2014 Apr 22:10:897-901. doi: 10.3762/bjoc.10.87. eCollection 2014.

Abstract

Unsymmetrically coupled biaryls are synthesized in high yield starting from different aryl bromides and bis(pinacolato)diboron by carrying out the Miyaura borylation reaction followed by the Suzuki-Miyaura reaction in the same reaction pot over 1-2 mol % SiliaCat DPP-Pd. The SiliaCat DPP-Pd catalyst is air-stable and the method does not require the use of inert conditions. The use of non-toxic isopropanol or 2-butanol as reaction solvent further adds to the environmental benefits of this new green synthetic methodology.

Keywords: SiliaCat; Suzuki–Miyaura; borylation; cross-coupling; one-pot.