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HRID 129638作成日:2026年10月27日
1,2-Dichloroethane → 2-(p-Chlorophenyl)-3-[(trifluoromethyl)sulfonyl]-5-[(trifluoromethyl)thio]pyrrole
https://huagongshe.com/reaction/129638
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1,2-Dichloroethane | HCID 11 | — |
| 反応物 | Trifluoromethanesulfonic acid | HCID 62406 | — |
| 反応物 | Methanesulfenyl chloride, trifluoro- | HCID 67900 | — |
| 反応物 | 2-(p-Chlorophenyl)-3-[(trifluoromethyl)sulfonyl]pyrrole | HCID 10448068 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 2-(p-Chlorophenyl)-3-[(trifluoromethyl)sulfonyl]-5-[(trifluoromethyl)thio]pyrrole | HCID 18930406 | 72% |
反応手順
A solution of 2-(p-chlorophenyl)-3-[(trifluoromethyl)sulfonyl]pyrrole (2.47 g, 0.0080 mol), trifluoromethylsulfenyl chloride (2.18 g, 0.016 mol), trifluoromethanesulfonic acid (0.12 g, 0.0008 mol) and 1,2-dichloroethane (15 mL) is placed in a pressure tube, heated at 70° C. for five days, diluted with methylene chloride, washed with saturated sodium hydrogen carbonate solution and brine, dried over anhydrous magnesium sulfate and concentrated in vacuo to obtain an amber syrup. Flash chromatography of the syrup using silica gel and a 1:5 ethyl acetate/hexanes solution gives the title product as an off-white solid (2.36 g, mp 118°-122° C.) which is identified by 1HNMR and 13CNMR spectral analyses.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05468877 |
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| 出典データセット | uspto-grants-1995_11 |
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| ORD ID | ord-266616786e864f3889254a00732a3a34 |
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| 出典メモ | uspto-grants-1995_11 |
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