Mild Conversion of β-Diketones and β-Ketoesters to Carboxylic Acids

摘要

A mild protocol for the conversion of β-ketoesters and β-diketones to carboxylic acids with use of CAN in CH_3CN is described. The method is compatible with a number of functional groups, and can generate carboxylic acids under neutral conditions at room temperature. The reaction is fast and general, providing an alternative method to the commonly used malonic ester acid preparation. Initial mechanistic studies show that initial oxidation of the enol form of the β-dicarbonyl initiates the reaction. The presence of nitrate as an oxidant ligand or as an additive is critical for success of the reaction.