A model reaction of o-(N-phenylcarbamoyl)benzoic acid (amic acid) with threefold amounts of 1-phenylethyl bromide (FEB) and 1,8-diazabicyclo-[5,4,0]-7-undecene (DBU) was carried out in NMP. The reaction gave N-[m-(1-phenylethoxycarbonyl)phenyl]phthalimide in al most quantitative yield at room temperature for 2 h. Polyimide containing pendant 1-phenylethyl ester (P-1a) was also prepared from polyamic acid with FEB using DBU according to the model reaction. The obtained polymer was exactly consistent with P-1a synthesized stepwise from the esterification of the corresponding polyimide containing pendant carboxylic acid with FEB. Therefore, the reaction of polyamic acid bearing pendant carboxylic acid with alkyl bromide proceeded quantitatively to give polyimide containing pendant ester in the presence of DBU. Also, this method was applied to the synthesis of polyimide containing l-phenylethyl ether. However, the polyimide with quantitative etherification was not synthesized. The acid-catalyzed deesterification of P-1a film was carried out by heating the irradiated polymer film containing 10 wt % of p-nitrobenzyl 9,10-diethoxyanthracene-2-sulfonate, which produced sulfonic acid by irradiation, at various temperatures. Although thermal deesterification of P-1a started at 220 degrees C without any acid catalyst, the deesterification occurred when the irradiated film was heated at the lower temperature. The degree of esterification can be determined from the disappearance of absorption at 700 cm(-1). The deesterification obeyed first-order kinetics.