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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242931Generated: October 31, 2026

Ammonium Chloride → 3-Chloro-4-fluoro-N2-phenylbenzene-1,2-diamine

https://huagongshe.com/reaction/242931

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant(2-Chloro-3-fluoro-6-nitrophenyl)phenylamineHCID 68156999—
CatalystIronHCID 23925—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product3-Chloro-4-fluoro-N2-phenylbenzene-1,2-diamineHCID 6815771381%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a mixture of (2-chloro-3-fluoro-6-nitrophenyl)phenylamine (1.28 g, 4.8 mmol) in MeOH (45 mL) and water (15 mL) were added NH4Cl (1.48 g, 28.8 mmol) and iron powder (1.07 g, 19.2 mmol) and the reaction mixture heated at 90° C. for 2 h. After cooling to RT, the crude mixture was filtered through a pad of Celite® and the filtrate concentrated in vacuo. The resulting residue was partitioned between EtOAc and water. The aqueous phase was extracted with EtOAc (×3) and the combined organic fractions washed with brine, dried (MgSO4) and concentrated in vacuo. The resulting residue was purified by column chromatography (Si—PCC, gradient 0-100% DCM in cyclohexane) to afford the title compound (918 mg, 81%). LCMS (Method C): RT 3.46 min [M+H]+ 237.1/239.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653089B2
Source datasetuspto-grants-2014_02
ORD IDord-af610b4edd2d4582b26a0f6716d4d887
Source noteuspto-grants-2014_02