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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120081Generated: October 26, 2026

2-Chloro-4-fluoro-5-nitrobenzoic Acid → 5-Amino-2-chloro-4-fluorobenzoic acid

https://huagongshe.com/reaction/2120081

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-4-fluoro-5-nitrobenzoic AcidHCID 7210828—
CatalystIronHCID 23925—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product5-Amino-2-chloro-4-fluorobenzoic acidHCID 12056784—

Reaction Steps

A solution of 2-chloro-4-fluoro-5-nitrobenzoic acid (18.0 g, 0.0824 mol) in 75 ml of acetic acid was heated at reflux temperature. Iron powder (18.4 g, 0.328 mol) was added in several portions and the resulting suspension was cooled to room temperature and diluted with water and ethyl acetate. The mixture was filtered and the filtrate was saved. The organic layer was washed with brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure to afford the title compound as a tan solid. Yield: 9.00 g (58.1%); mp.: 153-155° C.; identified by NMR and mass spectral analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06689773B2
Source datasetuspto-grants-2004_02
ORD IDord-43e77e092d3340a8976b25de0a9c5acc
Source noteuspto-grants-2004_02