摘要

Efficient oxidative cleavage of cinnamaldehyde to benzaldehyde catalyzed by metalloporphyrins in the presence of dioxygen has been developed. Manganese(III) meso-tetraphenylporphyrin chloride (MnTPPCl) showed excellent activity for the oxidation under mild conditions. Different influencing factors have been investigated, and 71% yield of benzaldehyde was obtained under the optimum conditions (60 degrees C, 3 h, toluene as solvent, molar ratio for cinnamaldehyde:MnTPPCl:isobutylaldehyde = 1:0.001:5). Moreover, a Plausible mechanism including free radical process and high-valent intermediate (Mn-IV=O) was proposed.