1-Bromo-2-fluorobenzene → 1-(2-Fluorophenyl)-2-phenylethan-1-one
Reaction equation
Br[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[F:8].ClC1C=C([C:17](=[O:25])[CH2:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)C=C(Cl)C=1>>[F:8][C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=1[C:17](=[O:25])[CH2:18][C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1Participants
3
Procedure
Prepared from 1-bromo-2-fluorobenzene following the procedure described in Intermediate 13, where the crude product was purified by column chromatography (PE:EtOAc=100:1) to afford Intermediate 24 (300 mg, yield 33.5%).
Workup
- customwas purified by column chromatography (PE:EtOAc=100:1)
Sources & evidence
- ORD record
- ord-f45c17d5f26b450bacad0cf2cfeaffd9
- Source dataset
- uspto-grants-2014_06
- Patent number
- US08741915B2
Reaction notes
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