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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

반응식

참여 물질

역할이름HCID투입량
반응물2-Trifluoromethylbenzenesulphonyl chlorideHCID 136616—
반응물Resorcinol, 5-methyl-, monohydrateHCID 3083941—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매Sodium BicarbonateHCID 516892—
생성물5-Methyl-3-(2-trifluoromethylphenylsulfonyloxy)phenolHCID 2272264955%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05891909
출처 데이터셋uspto-grants-1999_04
ORD IDord-86fabd4499e24b38aeff0345b47b251f
출처 메모uspto-grants-1999_04