HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64709Generated: October 28, 2026
Potassium isobutyrate → 16beta-Ethyl-17beta-isobutyryloxyacetoxy-4-estren-3-one
https://huagongshe.com/reaction/64709
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium isobutyrate | HCID 23677462 | — |
| Reactant | 16beta-Ethyl-bromoacetoxy-4-estren-3-one | HCID 86740980 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | 16beta-Ethyl-17beta-isobutyryloxyacetoxy-4-estren-3-one | HCID 70467307 | 70.8% |
Reaction Steps
In a mixture of 50 ml of acetone and 10 ml of water are dissolved 1.5 g of 16β-ethyl-bromoacetoxy-4-estren-3-one and 0.8 g of potassium isobutyrate and the solution is refluxed for 6 hours. The acetone is distilled off under reduced pressure and the residue is extracted with 200 ml of ethyl acetate. The organic layer is separated, washed with water and saturated aqueous sodium chloride and dried over anhydrous magnesium sulfate. The solvent is then distilled off under reduced pressure and the residue is subjected to column chromatography. Following passage of 100 ml of diisopropyl ether, elution is carried out with 300 ml of ethyl ether. The eluate is evaporated under reduced pressure to remove the solvent, giving 1.08 g of the above-identified compound as a viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04609650 |
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| Source dataset | uspto-grants-1986_09 |
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| ORD ID | ord-cdc3ce81002b4065be101e123cbaec2d |
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| Source note | uspto-grants-1986_09 |
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