Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Lithium | HCID 3028194 | — |
| Reactant | HCID 69625181 | HCID 69625181 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69917769 | HCID 69917769 | — |
Reaction Steps
x)—The alcohol obtained in the previous step (1.5 g) in dry tetrahydrofuran (24 ml) was added to a refluxing solution of lithium (2.12 g) in liquid ammonia (98 ml). After 4.5 h stirring at −35° C., 2-propanol was added in 30 min. and the ammonia was allowed to evaporate. Water was added and the product was extracted into ethyl acetate. The combined organic phases were washed with brine, dried over sodium sulfate and concentrated under reduced pressure, to give (7α,17β)-7-ethyl-3-methoxyestra-2,5(10),14-trien-17-ol (1.65 g) The product was used in the following step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06313108B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-86017154913e410d80a98e71d51e8e01 |
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| Source note | uspto-grants-2001_11 |
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