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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 887051Generated: October 26, 2026

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

https://huagongshe.com/reaction/887051

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 numberUS08247414B2
Source datasetuspto-grants-2012_08
ORD IDord-766088a8d3ac45c2a49b4edb14c80823
Source noteuspto-grants-2012_08