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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 64713Erstellt: 23. Oktober 2026

Octanoic Acid → 16beta-Ethyl-17beta-n-octanoyloxyacetoxy-4-estren-3-one

https://huagongshe.com/de/reaction/64713

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktOctanoic AcidHCID 379—
Edukt16beta-Ethyl-17beta-bromoacetoxy-4-estren-3-oneHCID 15593764—
LösungsmittelAcetoneHCID 180—
LösungsmittelWaterHCID 962—
LösungsmittelSodium HydroxideHCID 14798—
Produkt16beta-Ethyl-17beta-n-octanoyloxyacetoxy-4-estren-3-oneHCID 70466981—

Reaktionsschritte

In 60 ml of acetone is dissolved 1.0 ml of n-octanoic acid, and 3.0 ml of 2N-NaOH, 15 ml of water and 1.8 g of 16β-ethyl-17β-bromoacetoxy-4-estren-3-one are serially added to the above solution. The mixture is refluxed for 4 hours. The solvent is distilled off under reduced pressure and the residue is extracted with 150 ml of ethyl acetate. The organic layer is separated, washed with water and saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent is then distilled off under reduced pressure and the residue is subjected to column chromatography. Following passage of 50 ml of diisopropyl ether, elution is carried out with 300 ml of the same solvent. The eluate is evaporated under reduced pressure to remove the solvent, giving 1.7 g of the above-identified compound as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04609650
Quelldatensatzuspto-grants-1986_09
ORD IDord-fc929792369a463e95c40cc536834624
Quellennotizuspto-grants-1986_09