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HRID 9887作成日:2026年10月26日

1,4-Dioxane hydrochloride → Octahydroindolizin-7-one

https://huagongshe.com/reaction/9887

反応式

関与物質

役割名称HCID仕込み量
反応物1,4-Dioxane hydrochlorideHCID 20443148—
反応物(+/-)-1-(t-Butoxycarbonyl)-2-[4-(p-toluenesulfonyl)-2-oxobutyl]pyrrolidineHCID 21988484—
溶媒MethanolHCID 887—
生成物Octahydroindolizin-7-oneHCID 1124052465.3%

反応条件

温度50 °C

反応手順

(±)-1-(t-Butoxycarbonyl)-2-[4-(p-toluenesulfonyl)-2-oxobutyl]pyrrolidine (322 mg (0.814 mmol), prepared as described in 1)) was dissolved in methanol (3.2 ml). To the solution was added a solution of 4N hydrochloric acid/dioxane (0.61 ml, 2.44 mmol), and the resulting mixture was stirred at 50° C. for 30 minutes. At the end of this time, the reaction mixture was concentrated by evaporation under reduced pressure to remove solvents and any excess of hydrochloric acid. To the residue was added a saturated aqueous solution of sodium hydrogencarbonate and this was extracted with dichloromethane. The organic layer was washed with water, dried over anhydrous magnesium sulfate and the solvent was removed by distillation under reduced pressure. The residue was purified by column chromatography through alumina (eluent, ethyl acetate), to give the title compound (74 mg) as a light brown oil (yield 65%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091352B2
出典データセットuspto-grants-2006_08
ORD IDord-834874432cb64e90b07ca52638ef6387
出典メモuspto-grants-2006_08