HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2358276Generated: November 1, 2026
Methanol → 13-Methyl-1,8,11,12,13,14,15,16-octahydro-2H,6H-7-oxa-cyclopenta[a]phenanthrene-3,17-dione
https://huagongshe.com/reaction/2358276
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 3a-Methyl-6-(3-oxo-butyl)-1,2,4,5,9a,9b-hexahydro-3aH-9-oxa-cyclopenta[a]naphthalene-3,7-dione | HCID 68459875 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 13-Methyl-1,8,11,12,13,14,15,16-octahydro-2H,6H-7-oxa-cyclopenta[a]phenanthrene-3,17-dione | HCID 68457419 | — |
Reaction Steps
A 25% (w/w) solution of sodium methoxide in methanol (2.71 mL, 12.8 mmol, 1 eq) was added to a stirred solution of the crude 3a-Methyl-6-(3-oxo-butyl)-1,2,4,5,9a,9b-hexahydro-3aH-9-oxa-cyclopenta[a]naphthalene-3,7-dione in toluene (200 mL) at 0° C. The resulting mixture was stirred at 0° C. for 0.5 h. The reaction was then quenched with a 10:1 (v/v) of ammonium chloride/potassium bisulfate solution (100 mL). The aqueous layer was extracted with ethyl acetate (2×100 mL), and the combined organic layer was dried with magnesium sulfate. The resulting solution was filtered, evaporated and the residue purified by flash chromatography using 30-50% ethyl acetate in hexane to yield the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07763648B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-248325029a0e45e9bc1fd0bb91f7f565 |
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| Source note | uspto-grants-2010_07 |
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