HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196331Generated: October 29, 2026
Acetone → 6alpha,7alpha-Diepoxy-3-oxopregn-4-ene-20-carbaldehyde
https://huagongshe.com/reaction/1196331
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetone | HCID 180 | — |
| Reactant | Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) | HCID 466102 | — |
| Reactant | 6alpha,7alpha-Diepoxypregn-4-en-3one | HCID 86745798 | — |
| Product | 6alpha,7alpha-Diepoxy-3-oxopregn-4-ene-20-carbaldehyde | HCID 86745806 | 55% |
Reaction Steps
In 10 ml of acetone was dissolved 44.2 mg (0.1 mmole) of 20-(5,5-dimethyl-1,3-dioxan-2-yl)-1α,2α;6α,7α-diepoxypregn-4-en-3-one, followed by addition of 5 mg (0.02 mmole) of pyridinium p-toluenesulfonate. The mixture was refluxed for 2 hours. The reaction mixture thus obtained was cooled to room temperature and the solvent was distilled off under reduced pressure. The residue was diluted with methylene chloride and this methylene chloride solution was washed successively with saturated aqueous sodium hydrogen carbonate solution and saturated aqueous sodium chloride solution and dried over magnesium sulfate. The solvent was then distilled off under reduced pressure and the residue was purified by silica gel chromatography (eluent: ethyl acetate-hexane=1:5, v/v) to recover 19.6 mg of 1α,2α;6α,7α-diepoxy-3-oxopregn-4-ene-20-carbaldehyde (yield: 55%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05112998 |
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| Source dataset | uspto-grants-1992_05 |
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| ORD ID | ord-90c65a0f28dc4e67a8141a4d14e46d8b |
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| Source note | uspto-grants-1992_05 |
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