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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1756680Generated: October 29, 2026

HCID 10017173, compound → HCID 10315149, compound

https://huagongshe.com/reaction/1756680

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 10017173HCID 10017173—
SolventHydrochloric AcidHCID 313—
ProductHCID 10315149HCID 10315149161.6%

Reaction Steps

A solution of 1-acetyl-4-[3-(4-fluorobenzoyl)propyl]piperidine (1.7 g) in concentrated hydrochloric acid (15 ml) was refluxed for 16 hours and the hydrochloric acid was then distilled off under reduced pressure. The residue was dissolved in water and the solution was made weakly basic (pH ca.8) with 5% aqueous sodium hydroxide solution and extracted with dichloromethane. The extract was washed with water and dried over anhydrous sodium sulfate and the solvent was distilled off to recover 1.3 g of residue. To a solution of this residue (1.3 g) in ethanol (10 ml) was added 0.94 g of potassium carbonate and 0.9 g of benzyl bromide was added dropwise with ice-cooling. The mixture was stirred at room temperature for 2 hours and then filtered and the filtrate was concentrated under reduced pressure. The residue was diluted with water and extracted with dichloromethane and the extract was washed with water and dried over anhydrous sodium sulfate. Finally the solvent was distilled off to give 1.6 g of 1-benzyl-4-[3-(4-fluorobenzoyl)propyl]piperidine melting at 53°-55° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05441967
Source datasetuspto-grants-1995_08
ORD IDord-455b68f2bc5840959beb8c2733e74d8d
Source noteuspto-grants-1995_08