HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 64721Erstellt: 23. Oktober 2026
Sulfuric Acid → 16beta-Ethyl-17beta-(3-carboxypropyl)carbonyloxyacetoxy-4-estren-3-one
https://huagongshe.com/de/reaction/64721
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sulfuric Acid | HCID 1118 | — |
| Edukt | Glutaric anhydride | HCID 7940 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 16beta-Ethyl-17beta-glycoloyloxy-4-estren-3-one | HCID 70466441 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 16beta-Ethyl-17beta-(3-carboxypropyl)carbonyloxyacetoxy-4-estren-3-one | HCID 70467542 | 56,2% |
Reaktionsschritte
In 10 ml of dimethylformamide is dissolved 0.5 g of 16β-ethyl-17β-glycoloyloxy-4-estren-3-one, and 0.2 g of glutaric anhydride and then 0.3 ml of triethylamine are added to the above solution. The mixture is allowed to stand at room temperature (15°-25° C.) for 3 hours and poured into 20 ml of 10% aqueous sulfuric acid, followed by extraction with 100 ml of ethyl acetate. The organic layer is separated, washed with water and saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent is then distilled off under reduced pressure and the residue is subjected to column chromatography, elution being carried out with 200 ml of ethyl acetate. The eluate is evaporated under reduced pressure to remove the solvent, giving a colorless oil, which is allowed to stand to give 0.37 g of the above-identified compound as a solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04609650 |
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| Quelldatensatz | uspto-grants-1986_09 |
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| ORD ID | ord-8ad86bbd00414540bc192105b311a358 |
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| Quellennotiz | uspto-grants-1986_09 |
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