1-(1,1'-Biphenyl)-4-yl-2-phenylethan-1-one → 1-[4-(Morpholin-4-yl)phenyl]-2-phenylethanone
Reaction equation
Br[C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH2:13][CH2:12][O:11][CH2:10][CH2:9]2)=[CH:4][CH:3]=1.C1(C2C=CC=CC=2)C=CC([C:20](=[O:28])[CH2:21][C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)=CC=1>>[O:11]1[CH2:12][CH2:13][N:8]([C:5]2[CH:6]=[CH:7][C:2]([C:20](=[O:28])[CH2:21][C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=3)=[CH:3][CH:4]=2)[CH2:9][CH2:10]1Participants
3
Procedure
Prepared from 4-(4-bromophenyl)morpholine following the procedure described in Intermediate 14, where the crude product was purified by column chromatography (PE: EtOAc=5:1) to afford Intermediate 25 (280 mg, yield 36%).
Workup
- customwas purified by column chromatography (PE: EtOAc=5:1)
Sources & evidence
- ORD record
- ord-98c9229dc72e4f55be9cfd5fd3f5fa98
- Source dataset
- uspto-grants-2014_06
- Patent number
- US08741915B2
Reaction notes
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