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