Aminocarbonylations Employing Mo(CO)<sub>6</sub> and a Bridged Two-Vial System: Allowing the Use of Nitro Group Substituted Aryl Iodides and Aryl Bromides
作者:Patrik Nordeman、Luke R. Odell、Mats Larhed
DOI:10.1021/jo302322w
日期:2012.12.21
A bridged two-vial system aminocarbonylation protocol where Mo(CO)6 functions as an external in situ solid source of CO has been developed. For the first time both nitro group containing aryl/heteroaryl iodides and bromides gave good to excellent yields in the Mo(CO)6-mediated and palladium(0)-catalyzed conversion to benzamides, while the identical one-vessel protocol afforded extensive reduction of
A palladium-catalyzed, microwave assisted carbonylative reaction is described for the synthesis of benzamides fromarylbromides and primary or secondary amines. The developed method uses bis(cyclopentadienyldicarbonyliron) as a solid source of carbon monoxide to produce a diverse set of secondary and tertiary amides in 42–82% yield.