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HRID 7447作成日:2026年10月23日

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

https://huagongshe.com/ja/reaction/7447

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US07087594B2
出典データセットuspto-grants-2006_08
ORD IDord-c31ca254e6764d80bef08c91e727430e
出典メモuspto-grants-2006_08