HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1876737Generated: November 2, 2026
Water → (15alpha,16alpha)-15,16-Dihydro-3-methoxy-3′H-cycloprop[15,16]androsta-3,5,15-trien-17-one
https://huagongshe.com/reaction/1876737
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sulfoxonium, trimethyl-, iodide (1:1) | HCID 74498 | — |
| Reactant | (15alpha)-15-(Acetyloxy)-3-methoxyandrosta-3,5-dien-17-one | HCID 54571005 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | (15alpha,16alpha)-15,16-Dihydro-3-methoxy-3′H-cycloprop[15,16]androsta-3,5,15-trien-17-one | HCID 14031648 | — |
Reaction Steps
12.96 kg of trimethylsulfoxonium iodide is dissolved in 180 l of dimethyl sulfoxide under nitrogen bubbling and vigorous stirring and at 25-30° C. 5.51 kg of potassium hydroxide is added to the solution. Stirring is continued for 1 hour, then 16.22 kg of 15α-acetoxy-3-methoxyandrosta-3,5-diene-17-one is added, the reaction mixture is stirred at 25-30° C. until the reaction is complete (about 6 hours). The solution is added slowly to 900 l of water, the precipitate obtained is stirred for 30 minutes until it is dense, filtered by centrifuge, washed with portions of water until is neutral and dried in vacuo to constant weight at a temperature below 40° C. and the crude tide compound is crystallized from methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08309712B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-49ad37c4f9d043ebbf1a289c2e247868 |
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| Source note | uspto-grants-2012_11 |
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