Abstract: The disclosure relates to methods for electrochemical reductive carboxylation of an unsaturated organic substrate to form a dicarboxylic organic product. The unsaturated organic substrate is electrochemically reduced with a carbon dioxide reactant in an ionically conductive, water-immiscible reactant medium to form the dicarboxylic organic product. The dicarboxylic organic product is recovered in an aqueous product medium. Example dicarboxylic organic products include phthalic acid, naphthalenedicarboxylic acid, furan-2,5-dicarboxylic acid, thiophene-2,5-dicarboxylic acid, pyrrole-2,5-dicarboxylic acid, adipic acid, suberic acid, sebacic acid, and 1,12-dodecanedioic acid.

Abstract: The selective electrochemical reduction of halogenated 4-aminopicolinic acids is improved by activating the cathode at a final potential from about +1.0 to about +1.8 volts.

Abstract: A process for the preparation of ?-substituted carboxylic acids from the series including ?-hydroxycarboxylic acids and N-substituted-?-aminocarboxylic acids by cathodic carboxylation with carbon dioxide of a compound corresponding to the general formula R1—C(?X)R2 which is constituted by aldehydes, ketones or N-substituted imines. In the past, that carboxylation has taken place in an undivided electrolytic cell with the use of a sacrificial anode. As described herein, the carboxylation takes place in the absence of a sacrificial anode in an electrolytic cell divided by a separator, at a diamond film cathode. The anode is formed of a material which is stable under electrolytic conditions; in particular, it is a diamond film electrode. The catholyte includes an organic solvent and a conducting salt.

Abstract: A method for recuperating from saponification products of alkaline polyterephthalate with soda where both terephthalate ions are in acid form and the sodium ions are in the form of soda is disclosed. In this method the sodium terephthalate solution resulting from dissolving the saponification products are subjected to a step of electrochemical pre-acidification to bring the pH to 4 to 7. Thereafter an electrochemical acidification step by electrolysis is undertaken to precipitate the terephthalic acid in the anode section and recuperate the soda in the cathode section which can be recycled.

Abstract: The invention relates to a new process for the preparation of substituted diaminodicarboxylic acid derivatives of the formula ##STR1## in a high yield by a modified Kolbe synthesis.