ABSTRACT
An active catalyst, [Cu]@Ag composite, was synthesized for the first time and used as a cathode for electrocarboxylation of cinnamyl chloride with CO2. ß,γ-Unsaturated carboxylic acids were obtained with excellent yield and moderate selectivity. Moreover, reasonable yields and selectivities of carboxylic acids were also achieved with several allylic halides and aryl halides.
ABSTRACT
The electrocarboxylation of a series of benzophenones under galvanostatic conditions has been carried out in aprotic solvents using an undivided bulk electrolysis cell equipped with a Mg sacrificial anode. Systematic studies have been carried out in order to establish the qualitative relationships between the yield of carboxylation reaction and the operational and intrinsic parameters for the electrocarboxylation of benzophenones. For the diaryl ketones chosen for these studies, the yields of the target benzilic acids have been found to be strongly dependent on different parameters such as solvents, supporting electrolytes, cathode materials, current density, temperature and the nature of the substrates.