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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1294058Generated: November 1, 2026

p-Fluoronitrobenzene → Benzenamine, 2-nitro-4-(4-nitrophenoxy)-

https://huagongshe.com/reaction/1294058

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-FluoronitrobenzeneHCID 9590—
ReactantSodium hydrideHCID 24758—
Reactant4-Amino-3-NitrophenolHCID 3758882—
SolventDimethylformamideHCID 6228—
ProductBenzenamine, 2-nitro-4-(4-nitrophenoxy)-HCID 1203272283%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of 4-hydroxy-2-nitroaniline (3.08 g, 20.0 mmol) in DMF (30 mL) was added NaH (60% oily, 880 mg, 22.0 mmol) followed by 1-fluoro-4-nitrobenzene (2.33 mL, 22.0 mmol). The mixture was stirred at 90° C. overnight. After cooling, the mixture was extracted with ethyl acetate. The organic layer was washed with water and brine, dried over Na2SO4 then evaporated. Sequence purification on SiO2 column chromatography gave the title compound (4.56 g, 83%): MS m/e 274 (M−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238813B2
Source datasetuspto-grants-2007_07
ORD IDord-c2cbc1d491f14c8788e58d6cdfabb9d5
Source noteuspto-grants-2007_07