[CH3:1][C:2]1([CH3:15])[CH:7]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH2:6][CH2:5][C:4](=[O:14])[CH2:3]1.[Br:16]C1CC(C(C)C)CCC1=O>>[Br:16][CH:5]1[CH2:6][CH:7]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[C:2]([CH3:15])([CH3:1])[CH2:3][C:4]1=[O:14]The bromination of 3,3-dimethyl-4-phenyl-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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