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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2370951Generated: October 26, 2026

2-Bromo-1-fluoro-3,5-dinitrobenzene → 2-Bromo-3-fluoro-5-nitroaniline

https://huagongshe.com/reaction/2370951

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-1-fluoro-3,5-dinitrobenzeneHCID 58065778—
CatalystIronHCID 23925—
SolventAcetic AcidHCID 176—
SolventEthyl AcetateHCID 8857—
SolventSodium BicarbonateHCID 516892—
Product2-Bromo-3-fluoro-5-nitroanilineHCID 5806580652.6%

Reaction Steps

A mixture of 2-bromo-1,5-dinitro-3-fluorobenzene (100 mg, 0.38 mmol, 1 equiv) and iron powder (64 mg, 1.14 mmol, 3 equiv) in 3 mL of HOAc was stirred at room temperature for 90 minutes. The reaction mixture was diluted with EtOAc (20 mL) and saturated NaHCO3 (to ca. pH 7-8). The organic layer was separated and evaporated under vacuum. The crude residue was purified by column chromatography on silica gel using EtOAc/hexanes (1:4) as eluent to give 47 mg of 2-bromo-3-fluoro-5-nitroaniline (52%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710223B2
Source datasetuspto-grants-2014_04
ORD IDord-1033ae10ba9b4f00b74937dddb77dc43
Source noteuspto-grants-2014_04