HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27334Generated: October 25, 2026
Hydrochloric Acid → (17beta)-3-Oxoandrost-4-ene-17-carboxylic acid
https://huagongshe.com/reaction/27334
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Methyl (17beta)-3-oxoandrost-4-ene-17-carboxylate | HCID 165014 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (17beta)-3-Oxoandrost-4-ene-17-carboxylic acid | HCID 99472 | 98% |
Reaction Steps
To 2.462 kg. of methyl 4-androsten-3-one-17β-carboxylate in 24.6 l of methanol was added 1.23 kg. of potassium hydroxide in 4.9 l. of water. The reaction mixture was refluxed under nitrogen for 6 hours, and then allowed to cool to room temperature overnight. The mixture was acidified with 3200 ml. of 6 N hydrochloric acid. Most of the product crystallized as fine crystals. Then, 14 l. of water was added in a stream over 30 minutes, which precipitated all of the product. The mixture was aged with stirring for 4 hours at 30° C. The mixture was filtered on a cap funnel and washed with water until the wash water showed neutral. The product was dried in an oven at 50° C. overnight. The product, having a m.p. of 245°-248° C., was obtained in 98% yield (2.313 g.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04220775 |
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| Source dataset | uspto-grants-1980_09 |
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| ORD ID | ord-f656206c35324b4c97d16d00d8b85396 |
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| Source note | uspto-grants-1980_09 |
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