CC1CCCCC1=O.[C:9]([CH:13]1[CH2:18][CH2:17][CH2:16][CH:15]([Cl:19])[C:14]1=[O:20])(C)(C)C>>[Cl:19][CH:15]1[CH2:16][CH2:17][CH2:18][CH:13]([CH3:9])[C:14]1=[O:20]The chlorination of 2-methylcyclohexanone takes place in a manner similar to that described above for the preparation of 2-tert-butyl-6-chloro-cyclohexanone. The title compound is reacted as a crude product without further characterization.
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