Skip to Content
Merck
  • Oxygen-promoted PdCl2-catalyzed ligand-free Suzuki reaction in aqueous media.

Oxygen-promoted PdCl2-catalyzed ligand-free Suzuki reaction in aqueous media.

Organic & biomolecular chemistry (2010-12-15)
Chun Liu, Qijian Ni, Pingping Hu, Jieshan Qiu
ABSTRACT

A simple and efficient protocol has been developed for the PdCl(2)-catalyzed ligand-free and aerobic Suzuki reaction of aryl bromides or nitrogen-based heteroaryl bromides with arylboronic acids in good to excellent yields in aqueous ethanol. A systematic investigation on the effect of different atmospheres on the reactivity of the palladium-catalyzed Suzuki reaction has been carried out, the results show that an aerobic atmosphere demonstrates a positive effect on the reactivity of the Suzuki reaction in an aqueous media and a negative effect in a pure organic solvent, which exhibits that the water plays a crucial role for the function of the atmosphere on the palladium-catalyzed ligand-free Suzuki reaction.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Palladium(II) chloride solution, 5 wt. % in 10 wt. % HCl
Sigma-Aldrich
Palladium(II) chloride ChemBeads
Sigma-Aldrich
Palladium(II) chloride, ≥99.9%
Sigma-Aldrich
Palladium(II) chloride, anhydrous, 59-60% palladium (Pd) basis
Sigma-Aldrich
Palladium(II) chloride, anhydrous, 60% Pd basis
Sigma-Aldrich
Palladium(II) chloride, ReagentPlus®, 99%
Sigma-Aldrich
Palladium(II) chloride, 99.995%