참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Chlorosulfonic acid | HCID 24638 | — |
| 반응물 | Phosphorus oxychloride | HCID 24813 | — |
| 반응물 | Phosphorus pentachloride | HCID 24819 | — |
| 반응물 | 3-Methoxythiophene | HCID 140249 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 생성물 | 3-methoxythiophene-2-sulfonyl Chloride | HCID 11298822 | 43.4% |
반응 단계
Chlorosulfonic acid (ClSO3H, 2.31 g, 19.62 mmol) was slowly added at 0° C. to a solution of 3-methoxythiophene (2.29 g, 19.62 mmol) in CHCl3 (80 ml) 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).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05591761 |
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| 출처 데이터셋 | uspto-grants-1997_01 |
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| ORD ID | ord-260f0f7ab5354dafbb23a5e3d06e44bd |
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| 출처 메모 | uspto-grants-1997_01 |
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