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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726336Generated: October 30, 2026

Pyridine → 4-fluoro-N-(4-nitrophenyl)benzamide

https://huagongshe.com/reaction/726336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-NitroanilineHCID 7475—
Reactant4-Fluorobenzoyl chlorideHCID 67879—
CatalystPyridineHCID 1049—
Catalyst4-Fluorobenzoyl chlorideHCID 67879—
SolventDichloromethaneHCID 6344—
Product4-fluoro-N-(4-nitrophenyl)benzamideHCID 3948428100.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 30.0 gm (0.217 mole) 4-nitroaniline in 225 mL dichloromethane were added 17.57 mL (0.217 mole) pyridine. The suspension was cooled to 0° C. and then 25.66 mL (0.217 mole) 4-fluorobenzoyl chloride were added slowly. Within 15 minutes the reaction mixture became homogeneous and was allowed to warm to room temperature. After an hour an additional 2.56 mL (21.7 mMol) 4-fluorobenzoyl chloride and 1.75 mL (21.7 mMol) pyridine were added and the reaction continued at room temperature for an additional hour. The reaction mixture was then washed with 200 mL water at which point a precipitate formed. The solid was filtered, washed with 100 mL hexane, washed with 200 mL water and dried under reduced pressure at 60° C. to give 56.6 gm (100%) of the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05708187
Source datasetuspto-grants-1998_01
ORD IDord-04e59fadcc28436589d06bae735e3460
Source noteuspto-grants-1998_01