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HRID 1890749作成日:2026年10月23日

3-Sulfolene → 5-Bromo-2-(1,1-dioxo-tetrahydro-thiophen-3-yl)-1,2,3,4-tetrahydro-isoquinoline

https://huagongshe.com/ja/reaction/1890749

反応式

関与物質

役割名称HCID仕込み量
反応物3-SulfoleneHCID 6498—
反応物Potassium HydroxideHCID 14797—
反応物5-Bromo-1,2,3,4-tetrahydroisoquinoline hydrochlorideHCID 45074003—
溶媒WaterHCID 962—
溶媒Sodium BicarbonateHCID 516892—
生成物5-Bromo-2-(1,1-dioxo-tetrahydro-thiophen-3-yl)-1,2,3,4-tetrahydro-isoquinolineHCID 58317890—

反応条件

温度70 °C

反応手順

To a solution containing 5-bromo-1,2,3,4-tetrahydroisoquinoline hydrochloride (1.5 g, 6 mmol) and butadiene sulfone (1.2 g, 10.2 mmol) in water (20 mL) is added 1N KOH (10 mL). The reaction mixture is stirred at 70° C. for 24 hours. After cooling to ambient temperature, the reaction mixture is diluted with saturated NaHCO3 solution and extracted with dichloromethane three times. The organic phase is washed with brine and dried over Na2SO4 before drying by rotary evaporation. The crude product is purified by silica gel flash chromatography to afford 5-bromo-2-(1,1-dioxo-tetrahydro-thiophen-3-yl)-1,2,3,4-tetrahydro-isoquinoline as a wax-like solid. MS m/z 330.1 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08507491B2
出典データセットuspto-grants-2013_08
ORD IDord-978128e09c794bfa95ffcd1d26089dfe
出典メモuspto-grants-2013_08