HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 840185Generated: October 30, 2026
HCID 12149919, compound → HCID 70145734, compound
https://huagongshe.com/reaction/840185
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 12149919 | HCID 12149919 | — |
| Reactant | HCID 178435160 | HCID 178435160 | — |
| Reactant | HCID 178461633 | HCID 178461633 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 70145734 | HCID 70145734 | — |
Reaction Steps
Cuprous chloride (CuCl, 0.7611 g, 7.689 mmol) is slurried in THF (40 mL) under nitrogen and then chilled to −22° C. with a dry ice/tetrachloroethylene bath. Ethylmagnesium chloride solution (2.00 M in ether; 22.0 mL, 44.0 mmol) is added to the cold cuprous chloride slurry and the dark solution is stirred for 90 minutes. A solution of 3β-t-butyldimethylsilyloxy-androst-5,15-dien-17-one (from Example 28C;) in THF (50 mL) is added dropwise via polyethylene cannula to the organometallic solution over 10 minutes, followed by a THF rinse (20 mL). The reaction mixture is stirred for 2 hours at −22° C. and then allowed to warm to ambient temperature over 30 minutes, followed by addition of saturated aqueous NH4Cl (50 mL). The biphasic mixture is extracted with EtOAc (2×40 mL) and the combined organic layers are washed with brine (50 mL), dried over MgSO4, filtered and evaporated to dryness. Purification by flash chromatography gives 15β-ethyl-3β-t-butyldimethylsilyloxy-androst-5-en-17-one, which is deprotected as in Example 19C to give the corresponding 3-alcohol, which is then oxidized as in Example 16D to obtain the title compound, which has the following formula:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06365597B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-64af345b7a694fa79e0b3b44618d1e68 |
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| Source note | uspto-grants-2002_04 |
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