Aniline → 4-Bromo-2-nitroaniline
Reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5](F)=[C:4]([N+:9]([O-:11])=[O:10])[CH:3]=1.[NH2:12]C1C=CC=CC=1>CN(C=O)C>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([NH2:12])=[C:4]([N+:9]([O-:11])=[O:10])[CH:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 100 °C
Procedure
A mixture of 1-bromo-4-fluoro-3-nitrobenzene (2270 mg, 10.01 mol), aniline (3 ml) and DMF (20 ml) was heated at 100° C. under an atmosphere of Nitrogen for 7 h. The mixture was then concentrated in vacuo, and the residue triturated with heptane (30 ml) to give the desired product. 1H NMR (400 MHz, CDCl3) δ=7.11 (d, 1 H, J=9.2 Hz), 7.25-7.29 (m, 3 H), 7.40-7.45 (m, 3 H), 8.35 (d, 1 H J=2.4 Hz) and 9.45(brs, 1 H).
Workup
- concentrationThe mixture was then concentrated in vacuo
- customthe residue triturated with heptane (30 ml)
Sources & evidence
- ORD record
- ord-c35f46bc71bd4e16b1629a4931400f82
- Source dataset
- uspto-grants-2012_11
- Patent number
- US08314111B2
Reaction notes
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