4-Methyl-2-nitroaniline → 2-[(4-Methyl-2-nitroanilino)phenyl]ethanol
Reaction equation
[CH3:1][C:2]1[CH:8]=[CH:7][C:5]([NH2:6])=[C:4]([N+:9]([O-:11])=[O:10])[CH:3]=1.I[C:13]1[CH:18]=[CH:17][C:16]([CH2:19][CH2:20][OH:21])=[CH:15][CH:14]=1>>[CH3:1][C:2]1[CH:8]=[CH:7][C:5]([NH:6][C:15]2[CH:14]=[CH:13][CH:18]=[CH:17][C:16]=2[CH2:19][CH2:20][OH:21])=[C:4]([N+:9]([O-:11])=[O:10])[CH:3]=1Participants
3
Procedure
The title compound was prepared according to the procedure described in step 1 Example 45 from 4-methyl-2-nitroaniline and 4-iodophenylethyl alcohol.
Sources & evidence
- ORD record
- ord-7193b793d06d4cd4a961bbb2d190555f
- Source dataset
- uspto-grants-2009_01
- Patent number
- US07479564B2
Reaction notes
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