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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606382Generated: October 31, 2026

Potassium Hydroxide → 3beta-Hydroxy-5alpha-pregn-16-ene-11,20-dione

https://huagongshe.com/reaction/1606382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant3beta-Hydroxy-5alpha-pregn-16-ene-11,20-dione 3-acetateHCID 227102—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product3beta-Hydroxy-5alpha-pregn-16-ene-11,20-dioneHCID 7058342977.4%

Reaction Steps

A solution of 3β-acetoxy-5α-pregn-16-ene-11,20-dione (Chamberlin et al., J. Amer. Chem. Soc., 1951, 73, 2396) (25.7 g.) in dioxan (500 ml.) was treated with potassium hydroxide (10 g.) and water 250 ml. and the mixture allowed to stand at room temperature for 1 hour. After a further 1 hour at 40° the mixture was diluted with water and the product filtered off. The crude material was dissolved in chloroform and filtered through a column of grade III neutral alumina (ca. 100 g.). The material obtained was crystallised from acetone petroleum to give pure title compound (17.65 g.), as small plates, m.p. 217.5°, [α]D +82.9° (c 1.1), λmax. 234 nm. (ε 10,100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03952031
Source datasetuspto-grants-1976_04
ORD IDord-89775ab3fc2043ffa97a68a105710b62
Source noteuspto-grants-1976_04