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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1942148Generated: October 25, 2026

Water → 3-fluoro-N-(4-methoxyphenyl)-2-nitroaniline

https://huagongshe.com/reaction/1942148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantP-AnisidineHCID 7732—
ReactantPotassium CarbonateHCID 11430—
Reactant1,3-Difluoro-2-nitrobenzeneHCID 87922—
SolventDimethylformamideHCID 6228—
Product3-fluoro-N-(4-methoxyphenyl)-2-nitroanilineHCID 5510036364.2%

Reaction Conditions

Temperature75 °C

Reaction Steps

20.0 g (126 mmol) of 2,6-difluoronitrobenzene and 17.0 g (138 mmol) of p-anisidine were dissolved in N,N-dimethylformamide (60 ml), and 20.8 g (150 mmol) of potassium carbonate was added thereto. The mixture was heated with stirring for 12 hours at 75° C. The reaction mixture was poured into water, and extracted with ethyl acetate. The extracted organic layer was washed with water, 10% hydrochloric acid, water, and a saturated aqueous solution of sodium chloride in this order, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue thus obtained was purified by silica gel chromatography (developing solvent: ethyl acetate:hexane=1:9), to obtain 21.2 g (yield: 64%) of 3-fluoro-N-(4-methoxyphenyl)-2-nitroaniline as a brown liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389523B2
Source datasetuspto-grants-2013_03
ORD IDord-32478bc9497745548bc000700d20adbd
Source noteuspto-grants-2013_03