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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606383Generated: November 1, 2026

Dimethylformamide → 3alpha-Hydroxy-5alpha-pregn-16-ene-11,20-dione

https://huagongshe.com/reaction/1606383

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium AcetateHCID 517044—
Reactant3beta-Toluene-p-sulphonyloxy-5alpha-pregn-16-ene-11,20-dioneHCID 86733313—
SolventWaterHCID 962—
Product3alpha-Hydroxy-5alpha-pregn-16-ene-11,20-dioneHCID 5667332550.3%

Reaction Steps

A stirred mixture of 3β-toluene-p-sulphonyloxy-5α-pregn-16-ene-11,20-dione (627 g.), potassium acetate (918 g.), dimethylformamide (4.25 l.) and water (425 ml.) was heated on the steam bath for 4 hr. Most of the dimethylformamide was removed under reduced pressure and water was added to the residue with stirring. The solid (420 g.) was collected, washed and dried at 40° in vacuo. This material in peroxide free dioxan (7 l.) was flushed with nitrogen and a solution of potassium hydroxide (200 g.) in water (2 l.) was added. The mixture was stirred and heated at 50°-60° for 7 hr. and then left at room temperature overnight. Acetic acid (50 ml.) was added and the precipitated solid was filtered off, washed with water and dried. The dry solid was heated under reflux with benzene (2 l.) for 2 hr. the mixture cooled and filtered to give 3α-hydroxy-5α-pregn-16-ene-11,20-dione (215 g.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03952031
Source datasetuspto-grants-1976_04
ORD IDord-fa3c22caebc443b8aa1263b07616067d
Source noteuspto-grants-1976_04