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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2042622Generated: October 26, 2026

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

https://huagongshe.com/reaction/2042622

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 numberUS08586588B2
Source datasetuspto-grants-2013_11
ORD IDord-f3afc38c6a8744ad884b2a17a6fbe4f6
Source noteuspto-grants-2013_11