Acids, Dianhydrides, Isomerization cis-and rra«s-Dicyclohexyl-3,3',4,4'-tetracarboxylic acid and their dianhydrides were pre pared from tetramethyl dicyclohexyl-3,3',4,4'-tetra-carboxylates by hydrolysis and subse quent dehydration. The trans dianhydride 2b was found to be sensitive to temperature. Ho wever, once the imide ring is formed in the reaction with an amine, the model compound is thermostable. The products were characterized by ]H and 13C NMR, and also by two-dimen sional COSY spectroscopy. In the hydrolysis of c/s-tetramethyl dicyclohexyl-3,3',4,4'-tetracarboxylates in steam under high-pressure, rra/is-dicyclohexyl-3,3',4,4'-tetracarboxylic acid was formed, while the treatment of cw-dicyclohexyl-3,3',4,4'-tetracarboxylic acid in steam under high-pressure afforded also rran5,-dicyclohexyl-3,3',4,4'-tetracarboxylic acid. In a deuterium tracer experiment of cis-la, the 3,3',4,4'-tetradeuterated dicyclohexyl-3,3',4,4'-tetracarboxylic acid 2a was formed. An isomerization mechanism was postulated from this findings.