2-Methyl-3-nitroaniline → N-[4-(allyloxy)benzyl]-N-(2-methyl-3-nitrophenyl)amine
Reaction equation
[CH3:1][C:2]1[C:8]([N+:9]([O-:11])=[O:10])=[CH:7][CH:6]=[CH:5][C:3]=1[NH2:4].[CH2:12]([O:15][C:16]1[CH:23]=[CH:22][C:19]([CH:20]=O)=[CH:18][CH:17]=1)[CH:13]=[CH2:14]>>[CH2:12]([O:15][C:16]1[CH:17]=[CH:18][C:19]([CH2:20][NH:4][C:3]2[CH:5]=[CH:6][CH:7]=[C:8]([N+:9]([O-:11])=[O:10])[C:2]=2[CH3:1])=[CH:22][CH:23]=1)[CH:13]=[CH2:14]Participants
3
Procedure
2-Methyl-3-nitroaniline and 4-allyloxybenzaldehyde were processed as described in Example 1C to provide the title compound.
Sources & evidence
- ORD record
- ord-a57f914091f146cfac2b86679e82a9cd
- Source dataset
- uspto-grants-2003_06
- Patent number
- US06583180B2
Reaction notes
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