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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 601752생성일: 2026년 10월 25일

Lithium tri-tert-butoxyaluminohydride → Methyl 3-acetyloxy-12-hydroxydeoxycholan-24-ate

https://huagongshe.com/reaction/601752

반응식

참여 물질

역할이름HCID투입량
반응물Lithium tri-tert-butoxyaluminohydrideHCID 16710494—
반응물(R)-Methyl 4-((3R,5R,8R,9S,10S,13R,14S,17R)-3-acetoxy-10,13-dimethyl-12-oxohexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoateHCID 21632880—
용매TetrahydrofuranHCID 8028—
생성물Methyl 3-acetyloxy-12-hydroxydeoxycholan-24-ateHCID 1194464091.5%

반응 단계

A THF solution of lithium tri-tert-butoxyaluminum hydride (1 M, 22.4 mL, 22.4 mmol) was added drop wise to a solution of compound 2.0a (2.5 g, 5.6 mmol) in THF (25 mL) at ambient temperature. After stirring for an additional 4-5 h, the reaction was determined to be complete by TLC. The reaction was quenched by adding aqueous HCl (1 M, 10 mL) and the mixture was diluted with EtOAc (30 mL). The phases were separated and the organic phase was washed sequentially with water (15 mL) and saturated brine solution (10 mL). The organic phase was then dried over anhydrous Na2SO4 (3 g) and filtered. The filtrate was concentrated under vacuum and the resulting solid was purified by column chromatography [29 mm (W)×500 mm (L), 60-120 mesh silica, 50 g], eluting with EtOAc/hexane (2:8) [5 mL fractions, monitored by TLC with p-anisaldehyde charring]. The fractions containing the product were combined and concentrated under vacuum to provide compound 2.1a (2.3 g, 91%) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07902387B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-71b380fe8180429e96f5119d7132a7e9
출처 메모uspto-grants-2011_03