Aqueous DMF-potassium carbonate as a substitute for thallium and silver additives in the palladium-catalyzed conversion of aryl bromides to acetyl arenes

Highly selective palladium-catalyzed internal alpha -arylations of alkyl vi nyl ethers with aryl and heteroaryl bromides were conveniently conducted in aqueous DMF with potassium carbonate as base and with DPPP as bidentate li gand. The corresponding acetyl arene products were, after hydrolysis, isola ted in good to excellent yields. This Heck reaction procedure does not requ ire toxic thallium or expensive silver salt additives, is promoted by water , and is suggested to proceed via charged organopalladium intermediates. Si ngle-mode microwave irradiation was utilized in one example to shorten the reaction time.