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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 535667생성일: 2026년 10월 25일

4-Toluenesulfonyl chloride → 2-(6-Methoxypyridin-2-yl)ethyl 4-methylbenzenesulfonate

https://huagongshe.com/reaction/535667

반응식

참여 물질

역할이름HCID투입량
반응물4-Toluenesulfonyl chlorideHCID 7397—
반응물TriethylamineHCID 8471—
반응물2-(6-Methoxypyridin-2-yl)ethan-1-olHCID 15319871—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
생성물2-(6-Methoxypyridin-2-yl)ethyl 4-methylbenzenesulfonateHCID 59636776—

반응 단계

A solution of 2-(6-methoxypyridin-2-yl)ethanol (0.23 g, 1.50 mmol), 4-dimethylaminopyridine (0.028 g, 0.23 mmol), triethylamine (0.63 mL, 4.50 mmol) and p-toluenesulfonyl chloride (0.34 g, 1.80 mmol) in dry dichloromethane (5 mL) was stirred at rt over night. The solvent was removed in vacuo. Ethyl acetate and water were added. The organic phase was separated and the aqueous phase was extracted with ethyl acetate. The combined organic phases were dried (Na2SO4) and concentrated. The product was purified by flash chromatography (SiO2; heptane/EtOAc, gradient 0-100%). Yield: 0.18 g (38%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08859534B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-70334fdf56194307bd8210e70a762595
출처 메모uspto-grants-2014_10