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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196601Generated: October 30, 2026

Ethyl Acetate → HCID 19786595, compound

https://huagongshe.com/reaction/1196601

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactantp-Fluorophenyl 4-piperidyl ketone hydrochlorideHCID 3084438—
ReactantHCID 19786590HCID 19786590—
SolventWaterHCID 962—
ProductHCID 19786595HCID 1978659546.5%

Reaction Steps

To a solution consisting of 6,7-dihydro-5-dimethylaminomethyl-3-(2-fluorophenyl)-1,2-benzisoxazol-4(5H)-one hydrochloride (1.86 g) in distilled water (18.5 ml) was added 4-(4-fluorobenzoyl)piperidine hydrochloride (2.78 g) and potassium carbonate (0.80 g). The reaction mixture was heated at reflux for 3 hours. Upon cooling to room temperature, ethyl acetate was added and the layers were separated. The aqueous phase was extracted twice with ethyl acetate. The combined organic layers were washed with brine and dried (MgSO4). Filtration and concentration gave the crude product. Purification via flash column chromatography (silica gel, 40% ethyl acetate/hexane) PG,54 afforded 1.20 g of 6,7-dihydro-5-(4-(4-fluorobenzoyl)-1-piperidinyl)methyl-3-(2-fluorophenyl)-1,2-benzisoxazol-4(5H)-one. The compound was flushed through alumina with dichloromethane to give an oil which solidified on standing. The product was then recrystallized from ether/hexane, m.p. 99°-102° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05114936
Source datasetuspto-grants-1992_05
ORD IDord-77c2f8d927f9449986da85d3cb982b14
Source noteuspto-grants-1992_05