Bromobenzene → 4-[(3-Phenylpropyl)(2,2,2-trifluoroethyl)amino]-2-(trifluoromethyl)benzonitrile
Reaction equation
[CH2:1]([N:4]([CH2:17][C:18]([F:21])([F:20])[F:19])[C:5]1[CH:12]=[CH:11][C:8]([C:9]#[N:10])=[C:7]([C:13]([F:16])([F:15])[F:14])[CH:6]=1)[CH:2]=[CH2:3].Br[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1>>[C:23]1([CH2:3][CH2:2][CH2:1][N:4]([CH2:17][C:18]([F:19])([F:20])[F:21])[C:5]2[CH:12]=[CH:11][C:8]([C:9]#[N:10])=[C:7]([C:13]([F:14])([F:15])[F:16])[CH:6]=2)[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1Participants
3
Procedure
Synthesized according to Example 84B from 4-[2-propen-1-yl(2,2,2-trifluoroethyl)amino]-2-(trifluoromethyl)benzonitrile and bromobenzene: MS (El) m/z 386 (M+, 6%), 281 (84%), 197 (100%), 170 (76%).
Workup
- customSynthesized
Sources & evidence
- ORD record
- ord-76dd1651813d4e1bbbbc32a85ead5bc1
- Source dataset
- uspto-grants-2010_11
- Patent number
- US07834063B2
Reaction notes
Loading…