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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 58822생성일: 2026년 10월 24일

Hydrochloric Acid → Methanesulfonate

https://huagongshe.com/ko/reaction/58822

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물TriethylamineHCID 8471—
반응물Methanesulfonyl chlorideHCID 31297—
반응물Tetrahydro-3-furanmethanolHCID 139980—
용매DichloromethaneHCID 6344—
생성물MethanesulfonateHCID 85257—
생성물Tetrahydro-3-furanmethanolHCID 139980—

반응 조건

온도0 °C

반응 단계

Triethylamine (13.7 mL, 98 mmol) was added to a solution of tetrahydro-3-furanmethanol (10.0 g, 98 mmol) in methylene chloride (100 mL) at 0° C. followed by addition of methanesulfonyl chloride (12.3 g, 108 mmol) dropwise. The reaction mixture was stirred at 0° C. for 1 h and then allowed to warm to ambient temperature and stirred overnight. Aqueous hydrochloric acid (1N, 100 mL) was added and the two layers were separated. The organic layer was washed with 1N aqueous hydrochloric acid (100 mL×2), saturated aqueous sodium bicarbonate (100 mL×3), and brine (50 mL×1), respectively. The organic phase was dried over anhydrous sodium sulfate and concentrated to afford crude mesylate of tetrahydro-3-furanmethanol.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434761B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-75b92de63ae14e078729bd2eb9210720
출처 메모uspto-grants-2016_09