Reaction of Olefins with Malonic Acid Derivatives in the Presence of Manganese(III) Acetate

Abstract

Abstract The reaction of methylmalonic acid with mono- and disubstituted olefins in the presence of manganese(III) acetate yielded 2-carboxy-2-methyl-4-butanolides in moderate to good yields. The reactions of bromomalonic acid and chloromalonic acid with a variety of olefins gave 2-halo-4-butanolides and/or 2-buten-4-olides. The reaction of ethyl hydrogen malonate with olefins in the presence of manganese(III) acetate yielded 2-ethoxycarbonyl-2-buten-4-olides, 2-ethoxycarbonyl-2-ethenyl-4-butanolide, 2,7-dioxaspiro[4.4]nonane-1,6-diones, 2-ethoxycarbonyl-4-butanolide, and ethyl 3-butenoate. These reactions can be accounted for in terms of a free-radical mechanism involving substituted dicarboxymethyl radicals.