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HRID 1792358作成日:2026年10月27日

Sodium Hydroxide → 1-((2-Oxiranyl)methoxy)-2-(4,4,5,5,5-pentafluoropentylthio)ethane

https://huagongshe.com/reaction/1792358

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物(+)-EpichlorohydrinHCID 149428—
反応物2-(4,4,5,5,5-Pentafluoropentylthio)ethan-1-olHCID 22033252—
触媒t-Butylammonium hydrogen sulfateHCID 24996679—
生成物1-((2-Oxiranyl)methoxy)-2-(4,4,5,5,5-pentafluoropentylthio)ethaneHCID 2203322763%

反応条件

温度0 °C

反応手順

A mixture of 50% acqueous NaOH (1.85 ml), S-epichlorohydrin (1.142 g, 12.34 mmole) and t-butylammonium hydrogen sulfate (24 mg) was vigorously stirred at 0° C., for half an hour and allowed to reach room temperature. To this mixture was added 2-(4,4,5,5,5-pentafluoropentylthio)ethan-1-ol (735 mg, 3.08 mmole) at room temperature. The reaction mixture was stirred for 18 hours and quenched with water. The aqueous phase was extracted with ethyl acetate. Then, the organic layer was washed with water and saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was subjected to flash chromatography on silica gel (n-hexane:ethyl acetate=7:1) to give the title compound (568 mg, yield 63%) as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07074819B2
出典データセットuspto-grants-2006_07
ORD IDord-bc2e03d9f3304b1c8aa18d08880755d0
出典メモuspto-grants-2006_07