Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 442894생성일: 2026년 10월 25일
2-Trifluoromethylbenzenesulphonyl chloride → 5-Methyl-3-(2-trifluoromethylphenylsulfonyloxy)phenol
https://huagongshe.com/reaction/442894
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Trifluoromethylbenzenesulphonyl chloride | HCID 136616 | — |
| 반응물 | Resorcinol, 5-methyl-, monohydrate | HCID 3083941 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 용매 | Sodium Bicarbonate | HCID 516892 | — |
| 생성물 | 5-Methyl-3-(2-trifluoromethylphenylsulfonyloxy)phenol | HCID 22722649 | 55% |
반응 단계
Orcinol monohydrate (2.84 g, 20.0 mmol) and 2-trifluoromethylbenzenesulfonyl chloride (4.90 g, 20.0 mmol) were mixed in saturated aqueous NaHCO3 (70 mL) and diethyl ether (70 mL). The biphasic mixture was stirred vigorously at room temperature overnight. The reaction mixture was diluted with water (100 mL) and extracted into ethyl acetate (3×80 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 2% ethyl acetate in dichloromethane) to give the title compound as a white solid (3.65 g, 55%). 1H-NMR (300 MHz, CDCl3) δ 8.12 (d, J=8.0 Hz, 1 H), 7.98 (d, J=7.9 Hz, 1 H), 7.80 (t, J=8.2 Hz, 1 H), 7.69 (t, J=7.8 Hz, 1 H), 6.55 (s, 1 H), 6.48 (s, 1 H), 6.39 (s, 1 H), 5.11 (s, 1 H), 2.23 (s, 3 H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05891909 |
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| 출처 데이터셋 | uspto-grants-1999_04 |
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| ORD ID | ord-86fabd4499e24b38aeff0345b47b251f |
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| 출처 메모 | uspto-grants-1999_04 |
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