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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 255132생성일: 2026년 10월 25일

4-Toluenesulfonyl chloride → (R)-(tetrahydrofuran-2-yl)methyl 4-methylbenzenesulfonate

https://huagongshe.com/reaction/255132

반응식

참여 물질

역할이름HCID투입량
반응물4-Toluenesulfonyl chlorideHCID 7397—
반응물(2R)-oxolan-2-ylmethanolHCID 6931745—
용매PyridineHCID 1049—
용매DichloromethaneHCID 6344—
생성물(R)-(tetrahydrofuran-2-yl)methyl 4-methylbenzenesulfonateHCID 7033050—

반응 단계

To a solution of (R)-tetrahydrofurfuryl alcohol (Lancaster, 1.0 g, 9.8 mmol) in 5 mL of CH2Cl2 and 5 mL of pyridine was added p-toluenesulfonyl chloride (2.8 g, 15 mmol) portionwise 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 phase was extracted with three 5 mL portions of CH2Cl2. The combined organic extracts were dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure to afford the title compound. MS (DCI/NH3) m/z 257 (M+H)+, 274 (M+NH4)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07875639B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-e221c487392140d696e8d0ec88aad240
출처 메모uspto-grants-2011_01