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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081262Generated: November 2, 2026

Water → 2-Fluoro-n-(2-nitrophenyl)aniline

https://huagongshe.com/reaction/1081262

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-FluoroanilineHCID 9584—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Product2-Fluoro-n-(2-nitrophenyl)anilineHCID 261381—

Reaction Steps

A mixture of 2-fluoroaniline (5.0 g), potassium carbonate (2.5 g) and copper(I)iodide (414 mg) in 2-fluoronitrobenzene (16.9 ml) was heated to 180° under nitrogen for 18 h. The cooled mixture was poured into water (300 ml) and extracted with ethyl acetate (2×250 ml) then the combined extracts were washed with saturated brine and evaporated. The residual brown oil was azeotroped with ethanol/water then toluene. The residue was chromatographed with hexane-DE (100:0 to 95:5) to give the title compound (3.25 g) as a bright orange solid, m.p.58°-9°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05585376
Source datasetuspto-grants-1996_12
ORD IDord-6d09095ff529473ea1f7d148863cbfd3
Source noteuspto-grants-1996_12