Symmetrical dicarboxylic acids with 4-14 carbon atoms gave selectively the
corresponding monoesters in high yields in the transesterification catalyse
d by strongly acidic ion-exchange resins in ester-hydrocarbon mixtures. It
was found that the rate of the esterification of the dicarboxylic acids is
much higher than that of the monocarboxylic acids formed. This result can e
xplain the high selectivity for the monoester formation and can also be exp
lained by the existence of an aqueous layer on the surface of the resins. T
his method of selective esterification is quite simple and practical.