Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2-Methylbenzaldehyde | HCID 10722 | — |
| Edukt | Triphenylphosphine | HCID 11776 | — |
| Edukt | 2-Cyclohepten-1-one | HCID 70723 | — |
| Edukt | tert-Butyldimethylsilyl trifluoromethanesulphonate | HCID 123564 | — |
| Edukt | HCID 178418244 | HCID 178418244 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | HCID 69965728 | HCID 69965728 | — |
Reaktionsschritte
To a solution of cycloheptenone (71.7 mmol) in 220 ml of anhydrous THF there are added, in succession, triphenylphosphine (72.6 mmol) and then, dropwise, tert-butyldimethylsilyl triflate (72.3 mmol), and the whole is stirred at room temperature for 1 hour 30 minutes. The mixture is then brought to −78° C., and a solution of nBuLi/hexane (72 mmol) is added slowly, followed 30 minutes later by 2-methylbenzaldehyde (72.03 mmol). The whole is stirred at that temperature for 30 minutes, and then with the temperature gradually returning to room temperature. After 2 hours 30 minutes, the reaction mixture is precipitated from 2.5 liters of petroleum ether and filtered, and the filtrate is concentrated to dryness. The title product is purified by chromatography over silica gel (100% heptane).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US06638962B2 |
|---|
| Quelldatensatz | uspto-grants-2003_10 |
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| ORD ID | ord-1998a41d3c444e92befe8253cdc01e54 |
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| Quellennotiz | uspto-grants-2003_10 |
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