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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678951Generated: October 25, 2026

Acetic Acid → 19-Hydroxytestosterone

https://huagongshe.com/reaction/1678951

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantWaterHCID 962—
ReactantPotassium borohydrideHCID 4192641—
Reactant19-Hydroxy-4-androsten-3-oneHCID 22802257—
SolventEthanolHCID 702—
Product19-HydroxytestosteroneHCID 150968—

Reaction Conditions

Temperature0 °C

Reaction Steps

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 2 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 1 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 2 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04078060
Source datasetuspto-grants-1978_03
ORD IDord-5712b4f134514b2fabe48ee7b9e65655
Source noteuspto-grants-1978_03