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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 973216Generated: October 29, 2026

Acetic Acid → 19-Acetoxy-delta(sup 1)-testosterone

https://huagongshe.com/reaction/973216

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium borohydrideHCID 4311764—
Reactant19-Acetoxyandrost-4-en-3,17-dioneHCID 12942412—
SolventMethanolHCID 887—
Product19-Acetoxy-delta(sup 1)-testosteroneHCID 24833721—

Reaction Steps

To a solution of 25.6 g of 19-acetoxyandrost-4-ene-3,17-dione in 4 liters of methanol cooled to 0° C is added 3.1 g of sodium borohydride, and the mixture is stirred at 0° C for 1 hour after which 30 ml of acetic acid is added and the methanol removed under reduced pressure. The resulting residue is taken up in ethyl acetate and washed with water. The organic layer is dried over magnesium sulfate, filtered and the solvent removed. The solid residue is dissolved in 2 liters of chloroform treated with 125 g of manganese dioxide and stirred for 2 hours. The reaction mixture is filtered, and the solvent removed under reduced pressure. The residue is chromatagraphed on alumina using benzene-ether (1:1) as the eluant. The product is recrystallized from acetone-hexane to give 19-acetoxy-17β-hydroxyandrost-4-en-3-one, M.P. 125°-127° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04055641
Source datasetuspto-grants-1977_10
ORD IDord-72409447370b4252a3ef6a4922b459fc
Source noteuspto-grants-1977_10