4-Bromo-1,2-dichlorobenzene → 1-(3,4-Dichlorophenyl)-2-phenylethanone
Reaction equation
Cl[C:2]1[CH:3]=[C:4]([C:9](=[O:17])[CH2:10][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[CH:5]=[C:6]([Cl:8])[CH:7]=1.BrC1C=CC([Cl:25])=C(Cl)C=1>>[Cl:8][C:6]1[CH:5]=[C:4]([C:9](=[O:17])[CH2:10][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[CH:3]=[CH:2][C:7]=1[Cl:25]Participants
3
Procedure
Prepared following the procedure described in Intermediate 13, starting from 4-bromo-1,2-dichlorobenzene, where the crude product was purified by column chromatography (PE: EtOAc=100:1) to afford Intermediate 19 (230 mg, yield 42.4%).
Workup
- customPrepared
- customwas purified by column chromatography (PE: EtOAc=100:1)
Sources & evidence
- ORD record
- ord-3fbcb6e7481643aeb24915c1328fae43
- Source dataset
- uspto-grants-2014_06
- Patent number
- US08741915B2
Reaction notes
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