“…The preparation of cyclic acetals by azeotropic condensation has been described in a previous communication (34); the method is not applicable to the lowest-boiling representatives of the aliphatic ketones. It was, however, observed that the preparation of 2-methyl -2-ethyldioxolane from methyl ethyl ketone and ethylene glycol was much easier than literature data (35,36,37) would have led one to suspect. A mixture of 124 g. of glycol, 1152 g. of methyl ethyl ketone, 11.5 g. of gaseous hydrochloric acid, and 25 g. of anhydrous mag- " Procedure: To 0.25 mole of KOH (16.5 g. of technical potassium hydroxide) in the acetal was added a mixture of the hydrocarbon and the carbonyl compound at 20°.…”