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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696804Generated: November 3, 2026

Hydrochloric Acid → (3S)-1-(4-fluorobenzoyl)piperidine-3-carboxylic acid

https://huagongshe.com/reaction/1696804

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
Reactant4-Fluorobenzoyl chlorideHCID 67879—
Reactant(3S)-piperidine-3-carboxylic acid hydrochlorideHCID 24820453—
SolventDichloromethaneHCID 6344—
Product(3S)-1-(4-fluorobenzoyl)piperidine-3-carboxylic acidHCID 85867192.3%

Reaction Steps

To a suspension of (S)-piperidine-3-carboxylic acid hydrochloride (0.75 g, 4.53 mmol) in dry dichloromethane (30 mL), triethylamine (1.97 mL, 14.0 mmol) and 4-fluorobenzoyl chloride (543 mL, 4.53 mmol) were added dropwise at 0° C. The resulting solution was kept under stiffing overnight at room temperature, under nitrogen atmosphere, then HCl 1N (30 mL) was added and the phases were separated. The organic layer was washed with HCl 1N (30 mL), with water (30 mL), dried over Na2SO4 and evaporated under reduced pressure to provide 1.05 g of 1-(4-fluoro-benzoyl)-(S)-piperidine-3-carboxylic acid as a yellow oil, used for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163775B2
Source datasetuspto-grants-2012_04
ORD IDord-b6bc5218497e4a93b1f1f5ff8fe443a4
Source noteuspto-grants-2012_04