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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 442892생성일: 2026년 10월 26일

2-Chlorobenzenesulfonyl chloride → 3-(2-Chlorophenylsulfonyloxy)-5-methylphenol

https://huagongshe.com/reaction/442892

반응식

참여 물질

역할이름HCID투입량
반응물2-Chlorobenzenesulfonyl chlorideHCID 76187—
반응물Resorcinol, 5-methyl-, monohydrateHCID 3083941—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매Sodium BicarbonateHCID 516892—
생성물3-(2-Chlorophenylsulfonyloxy)-5-methylphenolHCID 1127794772%

반응 단계

Orcinol monohydrate (1.42 g, 10 mmol) and 2-chlorobenzenesulfonyl chloride (2.43 g, 11 mmol) were mixed in saturated aqueous NaHCO3 (30 mL) and diethyl ether (30 mL). The biphasic mixture was stirred vigorously at room temperature for 2 days. The reaction mixture was diluted with 50 mL of water 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 (2% ethyl acetate in dichloromethane) to give the title compound as a pale yellow liquid (2.15 g, 71%). 1H-NMR (300 MHz, CDCl3) δ 2.22 (s, 3 H), 5.24 (s, 1 H), 6.43 (s, 1 H), 6.52 (s, 2H), 7.38 (m, 1 H), 7.60 (m, 2 H), and 7.96 (dd, 1 H, J =0.6, 3.9 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05891909
출처 데이터셋uspto-grants-1999_04
ORD IDord-eff8a8e09e664107877f3bc4b771e78d
출처 메모uspto-grants-1999_04