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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2552생성일: 2026년 10월 23일

Water → cis-4-Tetrahydropyranyloxy 2-cyclopentenol

https://huagongshe.com/ko/reaction/2552

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물tert-Butyl methyl etherHCID 15413—
반응물Lithium hydroxide, monohydrateHCID 168937—
반응물(+)-Acetic acid cis-4-(tetrahydro-pyran-2-yloxy)-cyclopent-2-enyl esterHCID 13623284—
용매ChloroformHCID 6212—
용매Methanol tetrahydrofuran waterHCID 21892291—
생성물cis-4-Tetrahydropyranyloxy 2-cyclopentenolHCID 1362325293%

반응 단계

Dissolve (-)-acetic acid cis-4-(tetrahydro-pyran-2-yloxy)-cyclopent-2-enyl ester (106 mg, 0.47 mmol, prepared in example 11) in THF/methanol/water (1.5/0.5/0.5 mL). Add lithium hydroxide monohydrate (0.57 mmol) with stirring. After stirring for about 3 hours at room temperature, dilute the reaction with tert-butyl methyl ether (10 mL) and water (10 mL). Extract with tert-butyl methyl ether (2×10 mL). Combine the organic extracts, dry over anhydrous magnesium sulfate, filter and concentrate under vacuum. Purify the residue by flash chromatography (silica gel, 2.5 g, 1.7×2.5 cm column, 50% ethyl acetate/hexane, 150 mL) to provide the title compound (80 mg, 93% yield), [α]20D =+9.9°, (c=0.98, chloroform).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05728899
출처 데이터셋uspto-grants-1998_03
ORD IDord-73c1b39d43c34bba9c7f0a1fb0614d7e
출처 메모uspto-grants-1998_03