4-Aminophenethyl alcohol → 2-[4-(3,5-Dimethyl-2-nitroanilino)phenyl]ethanol
Reaction equation
[CH3:1][C:2]1[CH:7]=[C:6]([CH3:8])[C:5]([N+:9]([O-:11])=[O:10])=[C:4](F)[CH:3]=1.[NH2:13][C:14]1[CH:19]=[CH:18][C:17]([CH2:20][CH2:21][OH:22])=[CH:16][CH:15]=1>>[CH3:8][C:6]1[C:5]([N+:9]([O-:11])=[O:10])=[C:4]([CH:3]=[C:2]([CH3:1])[CH:7]=1)[NH:13][C:14]1[CH:19]=[CH:18][C:17]([CH2:20][CH2:21][OH:22])=[CH:16][CH:15]=1Participants
3
Procedure
The title compound was prepared according to the procedure described in step 3 of Example 1 from 4,6-dimethyl-2-fluoronitrobenzene and 4-aminophenylethyl alcohol.
Sources & evidence
- ORD record
- ord-641faa5ddb404bf98a4284bd28b7fe0b
- Source dataset
- uspto-grants-2011_04
- Patent number
- US07928119B2
Reaction notes
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