HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64708Generated: October 27, 2026
16beta-Ethyl-17beta-bromoacetoxy-4-estren-3-one → 16beta-Ethyl-17beta-propionyloxyacetoxy-4-estren-3-one
https://huagongshe.com/reaction/64708
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 16beta-Ethyl-17beta-bromoacetoxy-4-estren-3-one | HCID 15593764 | — |
| Reactant | Potassium propionate | HCID 23663619 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | 16beta-Ethyl-17beta-propionyloxyacetoxy-4-estren-3-one | HCID 13420414 | 35.4% |
Reaction Steps
In a mixture of 50 ml of acetone and 12 ml of water are dissolved 2.5 g of 16β-ethyl-17β-bromoacetoxy-4-estren-3-one and 0.7 g of potassium propionate. The solution is stirred at room temperature (17°-25° C.) for 3 days and concentrated under reduced pressure. 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 distilled off under reduced pressure and the residue is subjected to column chromatography. Following passage of 1000 ml isopropyl ether-n-hexane (2:3), elution is carried out with 2000 ml of the same solvent system. The eluate is evaporated under reduced pressure to remove the solvent, giving 0.87 g of the above-identified compound as white crystals.
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-a8f40c9d274a414588b143f5af3ffad3 |
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| Source note | uspto-grants-1986_09 |
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