Benzonitrile, 3-(bromomethyl)- → 3-{4-[(3-Cyanophenyl)methoxy]phenyl}-N-methylprop-2-enamide
Reaction equation
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]=[CH:9][C:10]([NH:12][CH3:13])=[O:11])=[CH:4][CH:3]=1.Br[CH2:15][C:16]1[CH:17]=[C:18]([CH:21]=[CH:22][CH:23]=1)[C:19]#[N:20]>>[C:19]([C:18]1[CH:17]=[C:16]([CH:23]=[CH:22][CH:21]=1)[CH2:15][O:1][C:2]1[CH:3]=[CH:4][C:5]([CH:8]=[CH:9][C:10]([NH:12][CH3:13])=[O:11])=[CH:6][CH:7]=1)#[N:20]Participants
3
Procedure
The title compound is prepared in analogy to example 11 b) from 3-(4-hydroxy-phenyl)-N-methyl-acrylamide and 3-bromomethyl-benzonitrile. Yield=75%. Colorless solid. MS: m/e=293.2 (M++H).
Sources & evidence
- ORD record
- ord-130f55bbee4e4e5b800fdf98d91a15bc
- Source dataset
- uspto-grants-2005_05
- Patent number
- US06900354B2
Reaction notes
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