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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1171148생성일: 2026년 10월 27일

tert-Butanol → (R)-4-((R)-benzyl-2-oxo-oxazolidin-3-yl)-3-(4-benzyloxy-2,6-dichloro-benzyl)-4-oxo-butyraldehyde

https://huagongshe.com/reaction/1171148

반응식

참여 물질

역할이름HCID투입량
반응물tert-ButanolHCID 6386—
반응물TetrahydrofuranHCID 8028—
반응물Sodium periodateHCID 23667635—
반응물(R)-4-benzyl-3-[(S)-2-(4-benzyloxy-2,6-dichloro-benzyl)-pent-4-enoyl]-oxazolidin-2-oneHCID 66671784—
촉매Osmium TetroxideHCID 30318—
용매WaterHCID 962—
생성물(R)-4-((R)-benzyl-2-oxo-oxazolidin-3-yl)-3-(4-benzyloxy-2,6-dichloro-benzyl)-4-oxo-butyraldehydeHCID 5951542948%

반응 단계

Treat a mixture of (R)-4-benzyl-3-[(S)-2-(4-benzyloxy-2,6-dichloro-benzyl)-pent-4-enoyl]-oxazolidin-2-one (0.96 g, 1.8 mmol), THF (21 mL) and water (7 mL) with 2.5% osmium tetroxide in t-butanol (46 mg, 0.18 mmol). Add sodium periodate (1.17 g, 5.5 mmol) and stir the reaction 4 hr at room temperature. Quench the reaction with water and extract with ethyl acetate. Wash the organic phase with aqueous 1N sodium thiosulfate then brine. Dry the organic layer over magnesium sulfate, filter, and concentrate under vacuum. Purify the crude material by silica gel chromatography using hexanes:ethyl acetate to elute the pure product. Concentrate the fractions containing product under vacuum to afford 0.46 g (48%) of desired product. MS (m/z): 526 (M+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07829582B2
출처 데이터셋uspto-grants-2010_11
ORD IDord-cc1a594997804137bc438540ad859fd5
출처 메모uspto-grants-2010_11