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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 328208Erstellt: 25. Oktober 2026

Hydrogen Peroxide → (17beta)-13-Ethyl-3-methoxygona-1,3,5(10),15-tetraen-17-ol

https://huagongshe.com/reaction/328208

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrogen PeroxideHCID 784—
EduktSodium borohydrideHCID 4311764—
Edukt16alpha,17alpha-Epoxy-3-methoxy-18-methyl-1,3,5(10)-estratrieneHCID 86734624—
EduktHCID 178528034HCID 178528034—
LösungsmittelEthanolHCID 702—
Produkt(17beta)-13-Ethyl-3-methoxygona-1,3,5(10),15-tetraen-17-olHCID 86734623—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

3.7 g. of diphenyldiselenide is dissolved in 200 ml. of absolute ethanol and combined at room temperature with 1.0 g. of sodium borohydride. After the yellow solution has lost its color, 5.0 g. of 16α,17α-epoxy-3-methoxy-18 -methyl-1,3,5(10)-estratriene is added thereto and the mixture is heated under reflux for 30 hours. The solution is then cooled to 0° C. Dropwise, 11ml. of 30% H2O2 is added to the reaction solution and the latter is then gradually heated to 50° C. After 2 hours, the solution is introduced into ice water. The precipitate is vacuum-filtered, washed with water, and taken up in methylene chloride. After chromatography on silica gel with 6-8% acetone/hexane, 1.9 g. of 3-methoxy-18-methyl-1,3,5(10),15-estratetraen-17α-ol is obtained as an oily product. [α]D 20 = -108°.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04016269
Quelldatensatzuspto-grants-1977_04
ORD IDord-47443581362643fe9d5aadc35279fb3a
Quellennotizuspto-grants-1977_04