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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033186Generated: October 25, 2026

Water → N-(2,5-Difluoro-4-nitrophenyl)acetamide

https://huagongshe.com/reaction/1033186

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAcetic AnhydrideHCID 7918—
Reactant2,5-Difluoro-4-nitroanilineHCID 235930—
CatalystSulfuric AcidHCID 1118—
Catalyst2-DimethylaminopyridineHCID 21885—
SolventDichloromethaneHCID 6344—
ProductN-(2,5-Difluoro-4-nitrophenyl)acetamideHCID 1462489388.4%

Reaction Steps

A mixture of 6.0 g (0.034 mole) of 2,5-difluoro-4-nitroaniline, 6.5 g (0.064 mole) of acetic anhydride, and approximately 0.1 g (0.0008 mole) of dimethylaminopyridine in 300 ml of methylene chloride was stirred and heated at reflux for two hours. The reaction mixture was allowed to cool and stir at room temperature for approximately 18 hours. The solvent was removed from the mixture by distillation under reduced pressure, leaving a residue. To this residue was added 32.5 g (0.318 mole) of acetic anhydride and several drops of concentrated sulfuric acid. This mixture was stirred at room temperature for approximately 18 hours. Approximately 300 ml of water was added to the mixture causing a vigorous exotherm and a solid to form. This solid was collected by filtration. The filter cake was washed with water and was dried under reduced pressure to yield 6.5 g of N-(2,5-difluoro-4-nitrophenyl)acetamide. The nmr spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05310724
Source datasetuspto-grants-1994_05
ORD IDord-577bd73ef8644ddb9ec7a279ccfeae41
Source noteuspto-grants-1994_05