Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1059461생성일: 2026년 10월 26일
2-Cyanobenzenesulfonyl Chloride → 3-[3-(2-Cyanophenylsulfonyloxy)-5-methylphenoxy]propanol Hydrochloride
https://huagongshe.com/reaction/1059461
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Cyanobenzenesulfonyl Chloride | HCID 522347 | — |
| 반응물 | Resorcinol, 5-methyl-, monohydrate | HCID 3083941 | — |
| 반응물 | 3-(2-Cyanophenylsulfonyloxy)-5-methylphenol | HCID 22722643 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 용매 | Sodium Bicarbonate | HCID 516892 | — |
| 생성물 | 3-[3-(2-Cyanophenylsulfonyloxy)-5-methylphenoxy]propanol Hydrochloride | HCID 18669705 | 57% |
반응 단계
3-(2-Cyanophenylsulfonyloxy)-5-methylphenol: Orcinol monohydrate (1.42 g, 10.0 mmol) and 2-cyanobenzenesulfonyl chloride (2.02 g, 10.0 mmol) were mixed in saturated NaHCO3 (30 mL) and diethyl ether (30 mL). The biphasic mixture was stirred vigorously at room temperature overnight. The reaction mixture was diluted with water (50 mL) and extracted into ethyl acetate (3×50 mL). The organic phase was washed with brine (2×50 mL) and dried over Na2SO4. After removing the solvent in vacuo, the residue was purified by flash column chromatography (dichloromethane to 5% ethyl acetate in dichloromethane) to give the title compound as a white solid (1.65 g, 57%). 1H-NMR (300 MHz, CDCl3) δ 8.07 (m, 1H), 7.94 (m, 1H), 7.75-7.80 (m, 2H), 6.57 (s, 1H), 6.53 (s, 1H), 6.49 (s, 1H), 5.69 (br s, 1H), 2.22 (s, 3H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06518310B2 |
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| 출처 데이터셋 | uspto-grants-2003_02 |
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| ORD ID | ord-b6531c9ea60c4c6a95928a78653eabc6 |
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| 출처 메모 | uspto-grants-2003_02 |
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