関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Chlorosulfonic acid | HCID 24638 | — |
| 反応物 | Phosphorus oxychloride | HCID 24813 | — |
| 反応物 | Phosphorus pentachloride | HCID 24819 | — |
| 反応物 | 3-Methoxythiophene | HCID 140249 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | 3-methoxythiophene-2-sulfonyl Chloride | HCID 11298822 | 43.4% |
反応手順
Chlorosulfonic acid (ClSO3H, 2.31 g, 19.62 mmol) was slowly added to a solution of 3-methoxythiophene (2.29 g, 19.62 mmol) in CHCl3 (80 ml) at 0° C. The resulting mixture was stirred at 0° C. for 30 min. The solvent was evaporated under reduced pressure at room temperature, the residue was suspended in POCl3 (15 ml, 156.96 mmol), and PCl5 (8.2 g, 39.24 mmol) was added slowly. The reaction was stirred at 60° C. for 18 h, then cooled to room temperature and poured onto crushed ice (200 g). The aqueous mixture was extracted with CHCl3 (2×150 ml) and the combined organic layers was dried (MgSO4). The solid was removed by filtration and the filtrate was concentrated to give 3-methoxy-2-thiophenesulfonyl chloride as a brown oil (1.81 g, 43% yield).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05594021 |
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| 出典データセット | uspto-grants-1997_01 |
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| ORD ID | ord-6c13f4bb83c240199d4200c43fc9398a |
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| 出典メモ | uspto-grants-1997_01 |
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