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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54313Generated: October 24, 2026

Water → 2-Bromo-4-fluoro-6-nitroaniline

https://huagongshe.com/en/reaction/54313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-bromobutanimideHCID 67184—
Reactant4-Fluoro-2-nitroanilineHCID 67769—
SolventDimethylformamideHCID 6228—
Product2-Bromo-4-fluoro-6-nitroanilineHCID 292004—

Reaction Steps

6-Bromo-4-fluoro-2-nitroaniline was prepared using an adaptation of the method of Mitchell et al., J. Org. Chem. 44:4733 (1979). To a solution of 4-fluoro-2-nitroaniline (500 mg, 3.2 mmol) in dry DMF (16 mL) under N2 was added dropwise a solution of N-bromosuccinimide (570 mg, 3.2 mmol) in dry DMF (16 mL). The reaction was allowed to stir 24 h. The solution was then poured into 100mL H2O and this aqueous phase extracted with 4×25 mL CH2Cl2. The combined organic phases were washed with 3×4 mL H2O and dried (MgSO4). The MgSO4 was vacuum filtered and the solvent rotary evaporated to yield a brown oil which crystallized on standing. 642 mg (85.4%). 1H NMR (CDCl3) δ6.51 (br s, 2H NH2), 7.58 (dd, JH4-3 =3 Hz, JH4-F =6.5 Hz, H-4), 7.92 (dd, JH3-4 =3 Hz, JH3-F =8.7 Hz, H-3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05622952
Source datasetuspto-grants-1997_04
ORD IDord-2c127c3d76424c8c9494c46b0a7809bd
Source noteuspto-grants-1997_04