참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | Oxalyl chloride | HCID 65578 | — |
| 반응물 | 4-(Pyrrolidin-1-YL)benzenesulfonic acid | HCID 22147101 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 4-(Pyrrolidin-1-yl)benzene-1-sulfonyl chloride | HCID 53415010 | 19% |
반응 단계
DMF (0.5 mL) was added to solution of 4-(pyrrolidin-1-yl)benzenesulfonic acid (7.3 g, 32.16 mmol) in dichloromethane (40 mL). Oxalyl chloride (10 g, 78.74 mmol) was then dropwise and the resulting solution was maintained at room temperature for 1 hour. The reaction mixture was then quenched by the addition of 40 mL of iced water. The resulting solution was extracted using dichloromethane (3×20 mL), and the organic layers were combined, dried (Na2SO4), filtered and concentrated. The residue was purified by column chromatography using a 1:100 ethyl acetate/petroleum ether solvent system to afford 1.5 g (19%) of 4-(pyrrolidin-1-yl)benzene-1-sulfonyl chloride as a yellow solid. 1H NMR (CDCl3) δ 7.78 (d, 2H), 6.55 (d, 2H), 3.41 (t, 4H), 2.03 (t, 4H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07696229B2 |
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| 출처 데이터셋 | uspto-grants-2010_04 |
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| ORD ID | ord-3aba208444d5408d908318debc6221c1 |
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| 출처 메모 | uspto-grants-2010_04 |
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