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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

반응식

참여 물질

역할이름HCID투입량
반응물2-Cyanobenzenesulfonyl ChlorideHCID 522347—
반응물Resorcinol, 5-methyl-, monohydrateHCID 3083941—
반응물3-(2-Cyanophenylsulfonyloxy)-5-methylphenolHCID 22722643—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매Sodium BicarbonateHCID 516892—
생성물3-[3-(2-Cyanophenylsulfonyloxy)-5-methylphenoxy]propanol HydrochlorideHCID 1866970557%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06518310B2
출처 데이터셋uspto-grants-2003_02
ORD IDord-b6531c9ea60c4c6a95928a78653eabc6
출처 메모uspto-grants-2003_02