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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9235생성일: 2026년 10월 23일

Hydrogen Peroxide → (z)-7-((1r,2s,3r)-3-Hydroxy-2-{3-[hydroxy-(1-propyl-cyclobutyl)-methyl]-phenyl}-5-oxo-cyclopentyl)-hept-5-enoic acid ethyl amide

https://huagongshe.com/ko/reaction/9235

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen PeroxideHCID 784—
반응물TetrahydrofuranHCID 8028—
반응물Ammonium ChlorideHCID 25517—
반응물Lithium tri-s-butylborohydrideHCID 3611392—
반응물(z)-7-((1r,2s,3r)-3-(Tert-butyl-dimethyl-silanyloxy)-2-{4-[(tert-butyl-dimethyl-silanyloxy)-cyclohexyl-methyl]-phenyl}-5-oxo-cyclopentyl)-hept-5-enoic acid methyl esterHCID 69367304—
반응물(z)-7-((1r,2s,3r,5s)-3-(Tert-butyl-dimethyl-silanyloxy)-2-{4-[(tert-butyl-dimethyl-silanyloxy)-cyclohexyl-methyl]-phenyl}-5-hydroxy-cyclopentyl)-hept-5-enoic acid methyl esterHCID 69367459—
생성물(z)-7-((1r,2s,3r)-3-Hydroxy-2-{3-[hydroxy-(1-propyl-cyclobutyl)-methyl]-phenyl}-5-oxo-cyclopentyl)-hept-5-enoic acid ethyl amideHCID 1195515893%

반응 조건

온도-78 °C

반응 단계

Representative procedure for reduction of the C9 ketone: (Z)-7-((1R,2S,3R,5S)-3-(tert-Butyl-dimethyl-silanyloxy)-2-{4-[(tert-butyl-dimethyl-silanyloxy)-cyclohexyl-methyl]-phenyl}-5-hydroxy-cyclopentyl)-hept-5-enoic acid methyl ester (6-1). L-selectride (300 μL, 0.3 mmol, 1 M/THF) was added to a −78° C. solution of ketone 5-3 (159 mg, 0.24 mmol) in 12 mL THF. The reaction was stirred for 30 min. at −78° C. and then 3% H2O2 (7 mL) was added. The reaction was stirred for 2 h at room temperature and then was poured into saturated NH4Cl solution. The mixture was extracted with ethyl acetate (3×50 mL) and the combined ethyl acetate solution was washed with brine and then was dried (Na2SO4), filtered and evaporated. Purification by flash chromatography on silica gel (8% ethyl acetate/hexanes) gave the title alcohol (149 mg, 93%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091231B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-56cee961749d4215a576198071e7b15b
출처 메모uspto-grants-2006_08