[Bmim]PF<sub>6</sub>‑Promoted Ligandless Suzuki–Miyaura Coupling Reaction of Potassium Aryltrifluoroborates in Water

Abstract

The Suzuki–Miyaura coupling reactions of potassium aryltrifluoroborates with aryl bromides in water are promoted by the addition of [bmim]­PF<sub>6</sub> using Pd­(OAc)<sub>2</sub> as a catalyst and Na<sub>2</sub>CO<sub>3</sub> as a base under air. The quantity of [bmim]­PF<sub>6</sub> used is crucial to the efficiency of the catalytic system. A wide range of biaryls and polyaryls can be easily prepared in good to excellent yields

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