1-Bromo-3,5-difluorobenzene → 3',5'-Difluoro-2-phenylacetophenone
Reaction equation
ClC1C=C([C:9](=[O:17])[CH2:10][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)C=C(Cl)C=1.Br[C:19]1[CH:24]=[C:23]([F:25])[CH:22]=[C:21]([F:26])[CH:20]=1>>[F:26][C:21]1[CH:20]=[C:19]([C:9](=[O:17])[CH2:10][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[CH:24]=[C:23]([F:25])[CH:22]=1Participants
3
Procedure
Prepared following the procedure described in Intermediate 13, starting from 1-bromo-3,5-difluorobenzene, where the crude product was purified by column chromatography (PE:EtOAc=100:1) to afford Intermediate 18 (100 mg, yield 10.3%).
Workup
- customPrepared
- customwas purified by column chromatography (PE:EtOAc=100:1)
Sources & evidence
- ORD record
- ord-fde73e07d37a46039d510173026ee8d6
- Source dataset
- uspto-grants-2015_06
- Patent number
- US09067893B2
Reaction notes
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