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HRID 442944생성일: 2026년 10월 25일

3-Chlorobenzenesulphonyl chloride → 3-(3-Chlorophenylsulfonyloxy)-5-methylphenol

https://huagongshe.com/reaction/442944

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참여 물질

역할이름HCID투입량
반응물3-Chlorobenzenesulphonyl chlorideHCID 17909—
반응물Resorcinol, 5-methyl-, monohydrateHCID 3083941—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매Sodium BicarbonateHCID 516892—
생성물3-(3-Chlorophenylsulfonyloxy)-5-methylphenolHCID 5401767969.6%

반응 단계

Orcinol monohydrate (1.42 g, 10.0 mmol) and 3-chlorobenzenesulfonyl chloride (2.21 g, 10.0 mmol) were mixed in saturated aqueous NaHCO3 (30 mL) and diethyl ether (30 mL). The biphasic mixture was stirred vigorously at ambient 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 2% ethyl acetate in dichloromethane) to give the title compound as a pale yellow oil (2.08 g, 69%). 1H-NMR (300 MHz, CDCl3) δ 7.86 (s, 1H), 7.74 (d, J=7.8 Hz, 1H), 7.64 (d, J=8.0 Hz, 1H), 7.48 (t, J=8.0 Hz, 1H), 6.57 (s, 1H), 6.40 (s, 1H), 6.33 (s, 1H), 5.32 (s, 1H), 2.24 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05891909
출처 데이터셋uspto-grants-1999_04
ORD IDord-fcbda711bffa48c3bb9d266f630745d4
출처 메모uspto-grants-1999_04