Relative esterifiability of the primary and secondary hydroxyl groups of glycerol

Summary A method has been devised for determining the relative esterifiability of the primary and secondary hydroxyl groups of glycerol. Contrary to the theory previously advanced by Feuge and Bailey, the primary and secondary hydroxyls are not equally esterifiable. The equilibrium constant favoring esterification of primary hydroxyl over secondary isca. 2.3 at reaction temperature (200°C.) and between 6 and 10 at room temperature. Since the equilibrium constant is substantially different at room temperature from that at reaction temperature, monoglycerides as customarily prepared are not at equilibrium at room temperature and undergo intramolecular migration of acyl groups frombeta toalpha hydroxyl positions. The rate of migration depends on the physical form of the ester and is accelerated by basic catalysts. In the vicinity of room temperature intermolecular rearrangement occurs only over very prolonged periods. The method of calculating relative esterifiability of primary and secondary hydroxyls should be applicable to other polyols.