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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 845604Generated: October 30, 2026

Hydrochloric Acid → (2-Fluorophenyl)(piperidin-4-yl)methanone--hydrogen chloride (1/1)

https://huagongshe.com/reaction/845604

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 13180319HCID 13180319—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product(2-Fluorophenyl)(piperidin-4-yl)methanone--hydrogen chloride (1/1)HCID 1318031340%

Reaction Steps

A solution of 40.5 g of 1-phenoxycarbonyl-4-(2-fluorobenzoyl)piperidine, 500 ml of ethanol and 500 ml of 30% of potassium hydroxide solution was stirred at a temperature slightly below reflux overnight. The reaction mixture was cooled to room temperature, diluted with 250 ml of water, and the ethanol partially removed under reduced pressure. The aqueous suspension was extracted with ether (2×150 ml) and the ether fraction subsequently extracted with 1N hydrochloric acid (2×200 ml). The aqueous solution was basified with 25% sodium hydroxide solution, extracted with ether (2×150 ml) and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure to give an oil. The oil was dissolved in a minimum amount of ethanol and a solution of ethereal hydrogen chloride was added dropwise until a precipitate formed. The solid was collected and dried to give 9.7 g (40%) of product. Recrystallization twice from ethanol-ether gave the analytical sample, mp 185°-187° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04758668
Source datasetuspto-grants-1988_07
ORD IDord-4f7c9af6a3064aef9312a3eeeef4231e
Source noteuspto-grants-1988_07