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Aldehydes and Ketones with Benzyl Alcohols and Amines 1875 acetone' and oxygen was bubbled through the solution for three days, acetone being added from time to time to replace that lost by evaporation. The solvent was evaporated and the solid residue extracted with a solution of potassium bicarbonate. Acidification of the carbonate solution, however, yielded no organic acid. Extraction of the residue with 5% sodium hydroxide yielded isodurenol melting at 78-79°.7 The only compound which (7) Hey, J. Chem. See., 1590 (1931). was isolated from the neutral fraction was unchanged enol (4.4 g.

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