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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49789Generated: October 25, 2026

Water → N-(1-benzoylpiperidin-4-yl)-4-fluorobenzamide

https://huagongshe.com/reaction/49789

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyridineHCID 1049—
ReactantBenzoyl chlorideHCID 7412—
Reactant4-fluoro-N-(piperidin-4-yl)benzamideHCID 4778226—
SolventDichloromethaneHCID 6344—
ProductN-(1-benzoylpiperidin-4-yl)-4-fluorobenzamideHCID 9797409—

Reaction Steps

To a suspension of N-(piperidin-4-yl)-4-fluorobenzamide (0.5 g) in dichloromethane (5 ml) were added pyridine (218 μl), dichloromethane (5 ml) and benzoyl chloride (290 μl) at ambient temperature. After stirring for 3.5 hours, water (5 ml) was poured into the mixture. An organic layer was separated, and washed with water and brine. After drying with magnesium sulfate, the solvents were removed under reduced pressure. A residue was purified by column chromatography (silica gel, toluene:ethyl acetate=1:1 to ethyl acetate). After rinse with diisopropyl ether, N-(1-benzoylpiperidin-4-yl)-4-fluorobenzamide (515 mg) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710043B1
Source datasetuspto-grants-2004_03
ORD IDord-64d0f593fc724881840098bfc8140046
Source noteuspto-grants-2004_03