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HRID 2377157作成日:2026年10月27日

Water → 1-(3-(2-(1-Benzothiophene-5-yl)ethoxy)propyl)-3-pyrrolidinol

https://huagongshe.com/reaction/2377157

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Potassium CarbonateHCID 11430—
反応物4-HydroxypyrrolidineHCID 98210—
反応物5-[2-(3-Chloropropyloxy)ethyl]benzo[b]thiopheneHCID 21990069—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物1-(3-(2-(1-Benzothiophene-5-yl)ethoxy)propyl)-3-pyrrolidinolHCID 2199003754.2%

反応条件

温度85 °C

反応手順

In 12 mL of N,N-dimethylformamide was dissolved 1.20 g of 5-[2-(3-chloropropoxy)ethyl]-1-benzothiophene, and 0.82 g of 3-pyrrolidinol and 1.30 g of potassium carbonate were added to the solution, after which the resulting mixture was stirred at 85° C. for 2.5 hours. After the reaction mixture was cooled, water and ethyl acetate were added thereto and the organic layer was separated. The organic layer was washed with water and then a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and then distilled under reduced pressure to remove the solvent. The residue was purified by a column chromatography (eluent; chloroform : methanol 20:1 to 10:1) to obtain 0.78 g of 1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-pyrrolidinol as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07468443B2
出典データセットuspto-grants-2008_12
ORD IDord-00ab880a920c4cc98bafb2f73b92c8a6
出典メモuspto-grants-2008_12