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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1675997생성일: 2026년 10월 26일

Ethyl Acetate → (S)-tert-butyl 5,6-dihydroxyhexanoate

https://huagongshe.com/reaction/1675997

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Sodium PyrosulfiteHCID 656671—
반응물Tert-butyl hex-5-enoateHCID 15047738—
반응물Water butanolHCID 22253497—
반응물1-((1R)-((2R,4R,5S)-5-ethylquinuclidin-2-yl)(6-methoxyquinolin-4-yl)methoxy)-4-((1R)-((2R,4S,5R)-5-ethylquinuclidin-2-yl)(6-methoxyquinolin-4-yl)methoxy)phthalazineHCID 51003674—
생성물(S)-tert-butyl 5,6-dihydroxyhexanoateHCID 58209443—

반응 조건

온도0 °C

반응 단계

To a suspension of AD-mix alpha (70 g) in water/butanol 1:1 (512 mL) cooled to 0° C., tert-butyl hex-5-enoate (8.5 g, 49.92 mmol) was added. The reaction mixture was stirred at 4° C. for 70 hrs. Then the reaction mixture was cooled to 0° C. and EtOAc (280 mL), followed by continuous portionwise addition of sodium metabisulfite (20.6 g). The mixture was stirred for 30 min at 0° C. and at rt for 1 hour. The organic layer was separated and the aqueous phase extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate and concentrated under reduced pressure. Chromatography over silica gel eluting with EtOAc 100% afforded the title compound as a pale yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08003811B2
출처 데이터셋uspto-grants-2011_08
ORD IDord-60648327a65642379848fb9f81480c4a
출처 메모uspto-grants-2011_08