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HRID 2304402作成日:2026年10月25日

Sodium Carbonate → (2R, 4R)-(+)-2-(ethoxycarbonyl)-4-hydroxy-1-(4-methoxy phenethyl) pyrrolidine

https://huagongshe.com/reaction/2304402

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物1-(2-Bromoethyl)-4-methoxybenzeneHCID 84427—
反応物Ethyl (2R,4R)-4-hydroxypyrrolidine-2-carboxylate hydrochlorideHCID 12709308—
触媒Sodium IodideHCID 5238—
溶媒AcetonitrileHCID 6342—
生成物(2R, 4R)-(+)-2-(ethoxycarbonyl)-4-hydroxy-1-(4-methoxy phenethyl) pyrrolidineHCID 5726939559.2%

反応条件

温度42.5 °C

反応手順

To a suspension of 6.60 g (33.7 mmol) of (2R, 4R)-(+)-2-(ethoxycarbonyl)-4-hydroxypyrrolidine hydrochloride in acetonitrile (60 ml) were added 8.22 g (77.6 mmol) of sodium carbonate, 4-methoxyphenethyl bromide (8.71 g, 40.5 mmol), and sodium iodide (150mg, 1.0 mmol) and the mixture was stirred at 40-45° C. for 65 h. The mixture was concentrated in vacuo and water was added to the residue, and the products were extracted with ethyl acetate. The extract was washed with saturated aqueous sodium chloride and the products were extracted with 10% aqueous hydrochloride. The extract was washed with ethyl acetate, basified with potassium carbonate and extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride, dried over anhydrous sodium sulfate, and concentrated in vacuo to obtain oily (2R, 4R)-(+)-2-(ethoxycarbonyl)-4-hydroxy-1-(4-methoxy phenethyl) pyrrolidine (5.85 g, 59.1%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06436922B1
出典データセットuspto-grants-2002_08
ORD IDord-6ccdb738df6b4affb83b91edc14ec7be
出典メモuspto-grants-2002_08