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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 78483생성일: 2026년 10월 26일

4-Toluenesulfonyl chloride → 2-(tetrahydro-2H-pyran-4-yl)ethyl 4-methylbenzenesulfonate

https://huagongshe.com/reaction/78483

반응식

참여 물질

역할이름HCID투입량
반응물4-Toluenesulfonyl chlorideHCID 7397—
반응물2-(Oxan-4-yl)ethan-1-olHCID 17750944—
용매PyridineHCID 1049—
용매DichloromethaneHCID 6344—
생성물2-(tetrahydro-2H-pyran-4-yl)ethyl 4-methylbenzenesulfonateHCID 59267964—

반응 단계

To a solution of 2-(tetrahydropyran-4-yl)-ethanol (1.5 g, 11.5 mmol) in 10 mL of CH2Cl2 and 7 mL of pyridine was added p-toluenesulfonyl chloride (2.4 g, 12.7 mmol) portion wise over 15 minutes. The mixture stirred at ambient temperature for 3 hours and was quenched with 10 mL of saturated, aqueous NaHCO3. The layers were separated and the aqueous layer was extracted with three 5 mL of portions of CH2Cl2. The combined organic extracts were dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. Purification via column chromatography (SiO2, 70% hexanes in ethyl acetate) afforded the title compound. MS (DCI/NH3) m/z 302 (M+NH4)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841334B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-f3b0d6ccd7d34ba098c8e6688887e93b
출처 메모uspto-grants-2014_09