Accéder au contenu
Merck

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
RÉSUMÉ

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.

MATÉRIAUX
Référence du produit
Marque
Description du produit

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