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-e8ca61853aff4f78805852f251cb860b
- Source dataset
- uspto-grants-2016_03
- Patent number
- US09283229B2
Reaction notes
Loading…