Water → 4-Bromo-2-nitroaniline
Reaction equation
[N+:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[NH2:10])([O-:3])=[O:2].C1C(=O)N([Br:18])C(=O)C1.O>CC(O)=O>[Br:18][C:8]1[CH:7]=[CH:6][C:5]([NH2:10])=[C:4]([N+:1]([O-:3])=[O:2])[CH:9]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 2-nitro-phenylamine (13.8 g, 100 mmol) in HOAc (150 mL) was added NBS (18 g, 101 mmol). The reaction mixture was stirred and heated to reflux over 1 hour. The cooled reaction mixture was poured into H2O (1000 mL) and stirred for 15 minutes. The resulting orange slurry was filtered and washed with H2O (300 mL) affording a 20.26 g (93%) of the title compound as a bright orange solid.
Workup
- temperatureheated
- temperatureto reflux over 1 hour
- customThe cooled reaction mixture
- stirringstirred for 15 minutes
- filtrationThe resulting orange slurry was filtered
- washwashed with H2O (300 mL)
Sources & evidence
- ORD record
- ord-9a4008ea87bc489ca8d325ccbbd74187
- Source dataset
- uspto-grants-2001_11
- Patent number
- US06313126B1
Reaction notes
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