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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 605225Generated: October 25, 2026

Benzoyl chloride → N-(4-fluoro-3-nitrophenyl)benzamide

https://huagongshe.com/reaction/605225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
Reactant4-Fluoro-3-nitroanilineHCID 67768—
SolventTetrahydrofuranHCID 8028—
ProductN-(4-fluoro-3-nitrophenyl)benzamideHCID 353522881.1%

Reaction Conditions

Temperature5 °C

Reaction Steps

To a solution of 4-fluoro-3-nitroaniline (2.00 g, 12.8 mmol) and Et3N (1.98 mL, 14.1 mmol) in THF (40 mL) was added benzoyl chloride (1.58 ml, 13.5 mmol) dropwise at 5° C. The mixture was stirred at 5° C. for 1 hour, warmed to room temperature, and then evaporated. The residue was suspended in H2O (100 ml), adjusted to pH 2, and then extracted with EtOAc. The extract was washed with H2O, 10% NaHCO3 and brine, dried over MgSO4, and concentrated under vacuum to give the crude product, which was purified by washing with i-Pr2O to give the title compound as pale brown crystal (2.70 g, 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910595B2
Source datasetuspto-grants-2011_03
ORD IDord-fc9411b66fab42c6a4fae27770980d1c
Source noteuspto-grants-2011_03