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HRID 221852作成日:2026年10月26日

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

https://huagongshe.com/reaction/221852

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物4'-HydroxyacetophenoneHCID 7469—
反応物Potassium CarbonateHCID 11430—
反応物N-(3-chloropropyl)piperidine hydrochlorideHCID 79624—
溶媒AcetoneHCID 180—
生成物AmmoniaHCID 222—
生成物1-[4-(3-Piperidin-1-ylpropoxy)phenyl]ethanoneHCID 22001126.8%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08207168B2
出典データセットuspto-grants-2012_06
ORD IDord-b682f420bbec46bfa892f79c2171f154
出典メモuspto-grants-2012_06