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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2058429Erstellt: 26. Oktober 2026

Acetic Acid → 19-Hydroxytestosterone

https://huagongshe.com/reaction/2058429

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktWaterHCID 962—
EduktPotassium borohydrideHCID 4192641—
Edukt19-Hydroxy-4-androsten-3-oneHCID 22802257—
LösungsmittelEthanolHCID 702—
Produkt19-HydroxytestosteroneHCID 150968—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A solution of 150 g of 19-hydroxyandrost-4-en-3-one in 6 liters of ethanol is cooled in an ice bath. To this cold solution is added 13.5 g of potassium borohydride, and the reaction mixture is stirred for two hours at about 0° C. after which a second 13.5 g or potassium borohydride is added. Two hours later a third 13.5 g portion of potassium borohydride is added to the reaction mixture which is stirred for an additional one hour then poured into 11 liters of water to which 70 ml of acetic acid is added. The ethanol is distilled off under reduced pressure and the aqueous residue cooled to 0° C. The solid which separates is filtered off, dried and dissolved in 25 liters of hot chloroform after which the temperature is adjusted to 25° C. To the chloroform solution is added 250 g of manganese dioxide, and the mixture is stirred for two hours then filtered and the solvents removed under reduced pressure. The solid residue is recrystallized from acetonitrile to give 17β,19-dihydroxyandrost-4-en-3-one. M.P. 205°-207° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04317818
Quelldatensatzuspto-grants-1982_03
ORD IDord-c2645277944145eb92e6f7f7c4a8b964
Quellennotizuspto-grants-1982_03