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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221852Generated: October 25, 2026

Sodium Iodide → 1-[4-(3-Piperidin-1-ylpropoxy)phenyl]ethanone

https://huagongshe.com/reaction/221852

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant4'-HydroxyacetophenoneHCID 7469—
ReactantPotassium CarbonateHCID 11430—
ReactantN-(3-chloropropyl)piperidine hydrochlorideHCID 79624—
SolventAcetoneHCID 180—
ProductAmmoniaHCID 222—
Product1-[4-(3-Piperidin-1-ylpropoxy)phenyl]ethanoneHCID 22001126.8%

Reaction Steps

A mixture of 5.97 g of 4′-hydroxyacetophenone (43.8 mmol), 13.0 g of 1-(3-chloropropyl)-piperidine hydrochloride (65.8 mmol), 12.70 g of potassium carbonate (91.89 mmol), and 3.28 g of sodium iodide (21.9 mmol) in 100 mL dry acetone was stirred at reflux. After 1.5 h, the reaction was cooled to room temperature, filtered and concentrated. Ethyl acetate was added and the white solid that remained was filtered off. The filtrate was concentrated in vacuo and the crude residue was purified via silica gel chromatography using a gradient of ethyl acetate then 400:20:10 ethyl acetate: 7N ammonia in methanol:methanol to yield 583 mg of 1-[4-(3-piperidin-1-ylpropoxy)phenyl]ethanone as an oil. MS m/z 265 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207168B2
Source datasetuspto-grants-2012_06
ORD IDord-b682f420bbec46bfa892f79c2171f154
Source noteuspto-grants-2012_06