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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | 3beta-Toluene-p-sulphonyloxy-5alpha-pregn-16-ene-11,20-dione | HCID 86733313 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3alpha-Hydroxy-5alpha-pregn-16-ene-11,20-dione | HCID 56673325 | 50.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03952031 |
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| Source dataset | uspto-grants-1976_04 |
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| ORD ID | ord-fa3c22caebc443b8aa1263b07616067d |
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| Source note | uspto-grants-1976_04 |
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