COBALT-CATALYZED LOW PRESSURE DOUBLE CARBONYLATION OF ARYL AND SECONDARY BENZYL HALIDES

Article abstract of DOI:10.1016/0022-328X(86)80020-1

α-Ketoacids can be easily synthesized with satisfactory yields and selectivities by carbonylation of aryl halides and secondary benzyl halides under very mild conditions.The reactions are catalyzed by Co2(CO)8 in alcoholic solvents; the presence of a methyl source (dimethyl sulfate or methyl iodide) is necessary for the carbonylation of the aryl halides.Base, temperature and solvent have large effects on the course of the reaction.