関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | (+)-Epichlorohydrin | HCID 149428 | — |
| 反応物 | 2-(4,4,5,5,5-Pentafluoropentylthio)ethan-1-ol | HCID 22033252 | — |
| 触媒 | t-Butylammonium hydrogen sulfate | HCID 24996679 | — |
| 生成物 | 1-((2-Oxiranyl)methoxy)-2-(4,4,5,5,5-pentafluoropentylthio)ethane | HCID 22033227 | 63% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07074819B2 |
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| 出典データセット | uspto-grants-2006_07 |
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| ORD ID | ord-bc2e03d9f3304b1c8aa18d08880755d0 |
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| 出典メモ | uspto-grants-2006_07 |
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