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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53698Generated: October 25, 2026

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

https://huagongshe.com/reaction/53698

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantChlorosuccinimideHCID 31398—
Reactant4-Fluoro-2-nitroanilineHCID 67769—
SolventDimethylformamideHCID 6228—
Product2-Chloro-4-fluoro-6-nitroanilineHCID 19958561—

Reaction Steps

2-Chloro-4-fluoro-6-nitroaniline was prepared using an adaptation of the method of Mitchell, et al. (Mitchell, R. H. et al., J. Org. Chem. 44: 4733 (1979)). To a solution of 4-fluoro-2-nitroaniline (500 mg, 3.2 mmol) in dry DMF (10 mL) under N2 was added dropwise a solution of N-chlorosuccinimide (426 mg, 3.2 mmol) in dry DMF (16 mL). The reaction was allowed to stir overnight. The solution was then poured into 100 mL H2O and the resulting cloudy suspension extracted with 4×25 mL ethyl acetate. The combined organic phases were washed with 4×25 mL H2O and 25 mL saturated NaCl solution and dried (MgSO4). The MgSO4 was vacuum filtered and the solvent rotary evaporated to yield a brown crystalline solid which was purified further by flash chromatography (2:1 hexanes:ethyl acetate) to yield 424 mg of an orange crystalline solid (69.5%) 1H NMR (CDCl3) δ 6.46 (br s, 2H, NH2), 7.42 (dd, JH5-3 =3 Hz, JH3-F =7.2 Hz, H-4), 7.85 (dd, JH5-3 =3 Hz, JH5-F =8.7 Hz, H-5)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05620979
Source datasetuspto-grants-1997_04
ORD IDord-4e3b15c66ebf45719cb89ad99ff610d7
Source noteuspto-grants-1997_04