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HRID 2042631作成日:2026年10月25日

Potassium Iodide → 6-[3-((R)-2-Methyl-pyrrolidin-1-yl)-propoxy]-3,4-dihydro-2H-naphthalen-1-one

https://huagongshe.com/reaction/2042631

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物Potassium CarbonateHCID 11430—
反応物6-(3-Chloro-propoxy)-3,4-dihydro-2H-naphthalen-1-oneHCID 22023232—
反応物(R)-2-methylpyrrolidine benzene sulfonateHCID 86646919—
溶媒AcetonitrileHCID 6342—
生成物6-[3-((R)-2-Methyl-pyrrolidin-1-yl)-propoxy]-3,4-dihydro-2H-naphthalen-1-oneHCID 59651963—

反応手順

In a 1 L round bottom flask, 6-(3-chloro-propoxy)-3,4-dihydro-2H-naphthalen-1-one (10.0 g, 41.9 mmol), benzenesulfonate (R)-2-methyl-pyrrolidinium (13.15 g, 84.0 mmol), potassium carbonate (23.15 g, 168 mmol), and potassium iodide (100 mg, 0.6 mmol) in acetonitrile (600 mL) was heated to reflux 14 h. The reaction was cooled and the solvent concentrated under vacuum. The slurry was partitioned between methylene chloride and water, then washed with water three times. The organics were extracted three times with 3% citric acid solution. The combined aqueous layers were basified with sat. NaHCO3 sol. and extracted with methylene chloride, then dried over MgSO4. Ethereal HCl was added and the solvents reduced under vacuum. Crystallization from MeOH/Et2O produced 8.75 g (65%). Mp 183-185° C. MS m/z=288 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08586588B2
出典データセットuspto-grants-2013_11
ORD IDord-9087f63e8b9f4adc909a11bed7076e5d
出典メモuspto-grants-2013_11