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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 553589생성일: 2026년 10월 24일

Tetrahydropyran-4-ylacetic acid → 2-(Oxan-4-yl)ethan-1-ol

https://huagongshe.com/ko/reaction/553589

반응식

참여 물질

역할이름HCID투입량
반응물Tetrahydropyran-4-ylacetic acidHCID 2773575—
반응물Aluminium lithium hydrideHCID 21226445—
용매TetrahydrofuranHCID 8028—
생성물2-(Oxan-4-yl)ethan-1-olHCID 1775094490.1%

반응 단계

To a suspension of 0.55 g of LiAlH4 (13.9 mmol) in THF (10 mL) is added dropwise a solution of 2 g (13.9 mmol) of (tetrahydro-pyran-4-yl)-acetic acid in THF (10 mL) under nitrogen atmosphere (CAUTION: highly exothermic reaction!). Upon complete addition, the reaction is stirred at room temperature for 18 h. The reaction is cooled in an ice-bath and quenched with addition of 1M aqueous NH4Cl solution (2 mL). The resulting precipitate is removed by filtration through Celite® and is rinsed with ethyl acetate (3×100 mL). The filtrate is dried over Na2SO4, filtered and concentrated under reduced pressure to afford 1.63 g of 2-(tetrahydro-pyran-4-yl)-ethanol as a colorless oil. Yield: 90%; ES-MS m/z 131 [M+H].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08048899B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-65fab71d1c714a8da636152c511b4be8
출처 메모uspto-grants-2011_11