Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Adamantanone | HCID 64151 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | HCID 15477419 | HCID 15477419 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22948017 | HCID 22948017 | 56% |
Reaction Steps
Phosphonate 8 (4.62 g, 14 mmol) and 2-adamantanone (2.58 g, 17 mmol) were dissolved in anhydrous THF (35 ml) under argon and cooled to -68° C. Dropwise addition of lithium diisopropylamide (18.6 mmol) in anhydrous THF (20 ml) at -68° C. generated the ylid, followed by subsequent olefination of the ketone. The reaction was slowly warmed to room temperature over 2 h and then stirred at 75° C. for 1 h. The solution was partitioned between EtOAc/NH4Cl, dried over Na2 SO4, evaporated and purified by silica gel chromatography (2% EtOAc/hexanes), yielding 2.5 g (55%) of enol ether 9 as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05840919 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-d7ea59e082a34f8bb84caefffe74fdea |
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| Source note | uspto-grants-1998_11 |
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