Phenol → 4-Bromo-N-methyl-2-nitro-3-phenoxyaniline
Reaction equation
[Br:1][C:2]1[CH:9]=[CH:8][C:5]([NH:6][CH3:7])=[C:4]([N+:10]([O-:12])=[O:11])[C:3]=1F.[C:14]1([OH:20])[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1>>[Br:1][C:2]1[CH:9]=[CH:8][C:5]([NH:6][CH3:7])=[C:4]([N+:10]([O-:12])=[O:11])[C:3]=1[O:20][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1Participants
3
Procedure
This compound was synthesized according to the procedure of Example 1, Step 1, using 4-bromo-3-fluoro-N-methyl-2-nitroaniline and phenol as the starting materials. LCMS calculated for C13H12BrN2O3 (M+H)+: m/z=323.0, 325.0. found: 322.9, 325.0.
Workup
- customThis compound was synthesized
Sources & evidence
- ORD record
- ord-c1a0929503084d6a83700e700684d8be
- Source dataset
- uspto-grants-2016_07
- Patent number
- US09399640B2
Reaction notes
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