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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 9239Erstellt: 23. Oktober 2026

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/de/reaction/9239

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrogen PeroxideHCID 784—
EduktAmmonium ChlorideHCID 25517—
EduktLithium tri-s-butylborohydrideHCID 3611392—
Edukt[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—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt[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%

Reaktionsschritte

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%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07091231B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-41d347d7d83e44799ee2817ae32e4c2a
Quellennotizuspto-grants-2006_08