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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1934668Generated: November 1, 2026

Dimethylformamide → 2-Fluoro-5-nitro-N-(phenylmethyl)benzamide

https://huagongshe.com/reaction/1934668

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantThionyl ChlorideHCID 24386—
Reactant2-Fluoro-5-nitrobenzoic acidHCID 280997—
SolventDichloromethaneHCID 6344—
Product2-Fluoro-5-nitro-N-(phenylmethyl)benzamideHCID 22467400—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 2-fluoro-5-nitrobenzoic acid (313 mg) in dichloromethane (4 mL) were added thionyl chloride (0.17 mL) and dimethylformamide (0.05 mL), and the mixture was heated for 36 hours under reflux. After evaporation of the solvent, the residue was dissolved in dichloromethane (4 mL). To this solution were added benzylamine (0.19 mL) and triethylamine (0.47 mL), and the mixture was stirred for 30 minutes at 0° C. After evaporation of the solvent, the residue was dissolved in ethyl acetate and washed successively with diluted hydrochloric acid, an aqueous sodium bicarbonate solution and brine. The organic layer was dried over sodium sulfate and evaporated in vacuo. The resulting residue was triturated with diisopropyl ether to give N-benzyl-2-fluoro-5-nitrobenzamide (436 mg) as a solid substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06384080B1
Source datasetuspto-grants-2002_05
ORD IDord-de41f020eb0344cfb69928742e3b8d7e
Source noteuspto-grants-2002_05