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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2559생성일: 2026년 10월 23일

Bicarbonate Ion → rac-(1R,4S)-4-hydroxycyclopent-2-en-1-yl acetate

https://huagongshe.com/ko/reaction/2559

반응식

참여 물질

역할이름HCID투입량
반응물Bicarbonate IonHCID 769—
반응물p-Toluenesulfonic acidHCID 6101—
반응물Carbonate IonHCID 19660—
반응물(+)-Acetic acid cis-4-(tetrahydro-pyran-2-yloxy)-cyclopent-2-enyl esterHCID 13623284—
용매EthanolHCID 702—
용매ChloroformHCID 6212—
생성물rac-(1R,4S)-4-hydroxycyclopent-2-en-1-yl acetateHCID 1015410375%

반응 단계

Dissolve (-)-acetic acid cis-4-(tetrahydro-pyran-2-yloxy)-cyclopent-2-enyl ester (192 mg, 0.85 mmol, prepared in example 11) in ethanol (1.5 mL) and treat with p-toluenesulfonic acid (11.7 mg). Stir the reaction at room temperature for 2 hours. Add carbonate or bicarbonate to neutralize the reaction mixture and concentrate under vacuum. Purify the residue by chromatography (silica gel, 3 g, 1.5×3 cm column, 33% ethyl acetate/hexane, 80 mL), to provide the title compound (90 mg, 75% yield, 91% ee), [α]20 D =-66.1°, (c=0.63, chloroform).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05728899
출처 데이터셋uspto-grants-1998_03
ORD IDord-4b9e268c96f04af98cb23843c3e81f50
출처 메모uspto-grants-1998_03