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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657115Generated: November 2, 2026

Potassium Iodide → HCID 19786565, compound

https://huagongshe.com/reaction/1657115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(4-Fluorobenzoyl)piperidineHCID 2724440—
ReactantHCID 19786564HCID 19786564—
SolventDimethylformamideHCID 6228—
ProductHCID 19786565HCID 1978656547.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution consisting of 5-(3-chloropropyl)-6,7-dihydro-3-methyl-1,2-benzisoxazol-4(5H)-one (0.85 g) and DMF (20 ml) was added anhydrous potassium carbonate (0.52 g) diisopropylethyl amine (0.33 ml), 4-(4-fluorobenzoyl)piperidine (0.92 g) and potassium iodide (62 mg) at room temperature with stirring. The flask was flushed with nitrogen and warmed to 80° C. for 24 hours. Upon cooling to room temperature, water and ethyl acetate were added to the reaction mixture. The layers were separated and the aqueous phase was extracted 3 times with ethyl acetate. The combined organic layers were washed with water twice, then brine. The organic phase was then dried (MgSO4), filtered, and concentrated to give the crude product. Purification via flash column chromatography (silica gel, 2% triethylamine/ether) afforded 0.70 g of 6,7-dihydro-5-[3-(4-(4-fluorobenzoyl)-1-piperidinyl)-propyl]-3-methyl -1,2-benzisoxazol-4(5H)-one as an oil which solidified on standing. The product was dissolved and flushed through alumina with dichloromethane. Recrystallization with ether/hexane gave the product as a solid, m.p. 81°-83° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05256672
Source datasetuspto-grants-1993_10
ORD IDord-c1a8830956cf467cb4ae4089961a665f
Source noteuspto-grants-1993_10