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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186885Generated: October 26, 2026

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

https://huagongshe.com/reaction/1186885

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 numberUS08673916B2
Source datasetuspto-grants-2014_03
ORD IDord-21040e98211c4c59838dd0fa594f5313
Source noteuspto-grants-2014_03