Benzyl Bromide → N,N-dibenzyl-N-(3-nitro-2-vinylphenyl)amine
Reaction equation
[N+:1]([C:4]1[C:5]([CH:11]=[CH2:12])=[C:6]([CH:8]=[CH:9][CH:10]=1)[NH2:7])([O-:3])=[O:2].[CH2:13](Br)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1>>[CH2:13]([N:7]([CH2:11][C:5]1[CH:6]=[CH:8][CH:9]=[CH:10][CH:4]=1)[C:6]1[CH:8]=[CH:9][CH:10]=[C:4]([N+:1]([O-:3])=[O:2])[C:5]=1[CH:11]=[CH2:12])[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1Participants
3
Procedure
The product from Example 44B and benzyl bromide were processed as described in Example 2A to provide the title compound.
Sources & evidence
- ORD record
- ord-a127b4b6c43c4d31a93164e36f0f7e84
- Source dataset
- uspto-grants-2003_06
- Patent number
- US06583180B2
Reaction notes
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