Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Cyclohexanone | HCID 7967 | — |
| Reactant | Aluminum isopropoxide | HCID 11143 | — |
| Reactant | 3-Methoxy-estra-2,5(10)-dien-17-ol | HCID 16752606 | — |
| Catalyst | 2,6-Di-tert-butyl-4-methylphenol | HCID 31404 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-Methoxyestra-2,5(10)-dien-17-one | HCID 22791425 | 87% |
Reaction Steps
To a stirred solution of 106.3 g (0.52 mmol) of aluminum isopropoxide in 2000 ml of dry toluene 720 ml of cyclohexanone, 0.35 g of 2,6-ditert-butyl-4-methyl-phenol and 100 g (0.307 mol) 3-methoxy-17-hydroxy-estra-2,5(10)-diene were added, then the reaction mixture was stirred at 108-110° C. for 1 h. The reaction was followed by TLC. After completion of the reaction the mixture was cooled to 20-25° C., 200 ml of water was added and the so obtained mixture was stirred for 1 h. The precipitated aluminum hydroxide was filtered off and the filtrate was concentrated to a volume of 250 ml under reduced pressure. A mixture of 200 ml of methanol and 100 ml of water was added to this concentrated warm—about 60° C.—solution, the obtained suspension was cooled to 20-25° C. and stirred for 1 h. The precipitated crystalline product was filtered off and dried below 40° C. in vacuum to yield 76.4 g (87%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08314145B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-96227a8b2b07442782f7117f5cad8a6e |
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| Source note | uspto-grants-2012_11 |
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