In connection with other synthetic work we had need to prepare laboratory quantities of the interesting polyketone leuconic acid (cyclopentanepentone pentahydrate, I). In 1921 Contardi1 reported that oxidation of myo-inositol (II) with nitric acid gives leuconic acid directly. Subsequently Gelormini and Artz2 showed that the reaction affords a complex mixture of products containing only small amounts of leuconic acid. The stepwise oxidation of myo-inositol, however, represents a convenient and inexpensive route to leuconic acid.