C([O:4][C:5](=[CH:7][C:8]([CH3:10])=[CH2:9])[CH3:6])(=O)C.[CH3:11][C:12]([CH3:16])=[CH:13][CH2:14]O.CC(C)=CC(O)=O>C(O)(=O)C>[CH3:6][C:5]([CH2:4][CH2:14][CH:13]=[C:12]([CH3:16])[CH3:11])=[CH:7][C:8](=[O:9])[CH3:10]110 parts of 4-methyl-2,4-pentadien-2-yl acetate and 60 parts of prenol are heated with 1.4 parts of 3,3-dimethylacrylic acid at about 180°C for 4 hours in a small pressure column at a pressure of 2 atmospheres, the acetic acid formed being distilled off continuously. Fractional distillation of the reaction product gives 61.8 parts of 4,8-dimethyl-3,7-nonadien-2-one (yield 86% of theory, conversion 62% based on prenol).
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