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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1020136Generated: October 30, 2026

Dimethylformamide → 2-Fluoro-4-nitrobenzamide

https://huagongshe.com/reaction/1020136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantOxalyl chlorideHCID 65578—
Reactant2-Fluoro-4-nitrobenzoic acidHCID 302679—
SolventDichloromethaneHCID 6344—
Product2-Fluoro-4-nitrobenzamideHCID 21784094—

Reaction Steps

To 2-fluoro-4-nitrobenzoic acid suspended in CH2Cl2 under Ar was added DMF then oxalyl chloride. The reaction was stirred at room temperature 1.5 h then the solvent was evaporated. The residue was dissolved in THF and ammonia gas was bubbled through the reaction for 15 min. The solvent was evaporated and the residue partitioned between EtOAc and water. The aqueous layer was extracted with EtOAc. The extracts were dried (MgSO4), filtered, and evaporated. Column chromatography (SiO2, 0-100% EtOAc/Hex) gave pure 2-fluoro-4-nitrobenzamide (E335).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716310B2
Source datasetuspto-grants-2014_05
ORD IDord-63569cfd228e437dbf95fc615ed957d4
Source noteuspto-grants-2014_05