[CH3:1][C:2]1([CH3:9])[CH2:7][CH2:6][CH2:5][CH2:4][C:3]1=[O:8].[Br:10]C1CC(C(C)C)CCC1=O>>[Br:10][CH:4]1[C:3](=[O:8])[C:2]([CH3:9])([CH3:1])[CH2:7][CH2:6][CH2:5]1The bromination of 2,2-dimethyl-cyclohexanone takes place in a manner similar to that described above for the preparation of 2-bromo-4-isopropyl-cyclohexanone. The title compound is reacted as a crude product without further characterization.
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