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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9239생성일: 2026년 10월 23일

Hydrogen Peroxide → [4-((1r,2s,3r,5s)-3-(Tert-butyl-dimethyl-silanyloxy)-2-{4-[(tert-butyl-dimethyl-silanyloxy)-cyclohexyl-methyl]-phenyl}-5-hydroxy-cyclopentyl)-but-2-ynyloxy]-acetic acid methyl ester

https://huagongshe.com/ko/reaction/9239

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen PeroxideHCID 784—
반응물Ammonium ChlorideHCID 25517—
반응물Lithium tri-s-butylborohydrideHCID 3611392—
반응물[4-((1r,2s,3r)-3-(Tert-butyl-dimethyl-silanyloxy)-2-{4-[(tert-butyl-dimethyl-silanyloxy)-cyclohexyl-methyl]-phenyl}-5-oxo-cyclopentyl)-but-2-ynyloxy]-acetic acid methyl esterHCID 91117818—
용매TetrahydrofuranHCID 8028—
생성물[4-((1r,2s,3r,5s)-3-(Tert-butyl-dimethyl-silanyloxy)-2-{4-[(tert-butyl-dimethyl-silanyloxy)-cyclohexyl-methyl]-phenyl}-5-hydroxy-cyclopentyl)-but-2-ynyloxy]-acetic acid methyl esterHCID 9160451761.9%

반응 단계

L-selectride (0.76 mL, 0.76 mmol, 1 M/THF) was added to a −78° C. THF (20 mL) solution of 10-3 (415 mg, 0.63 mmol). The reaction was stirred for 1 h and then 3% H2O2 (14 mL) was added. The resulting mixture was stirred at room temperature for 45 min. and then saturated NH4Cl solution (60 mL) was added. The resulting mixture was extracted with ethyl acetate (3×40 mL) and the combined ethyl acetate solution was washed with brine. The solution was then dried (Na2SO4), filtered and evaporated. Purification by flash chromatography on silica gel (25% ethyl acetate/hexanes) gave the title alcohol (255 mg, 0.39 mmol, 61%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091231B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-41d347d7d83e44799ee2817ae32e4c2a
출처 메모uspto-grants-2006_08