Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Boron trifluoride etherate | HCID 8000 | — |
| Edukt | 2-(Trimethylsiloxy)-1,3-butadiene | HCID 554657 | — |
| Edukt | HCID 58198117 | HCID 58198117 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | HCID 58197608 | HCID 58197608 | 52,1% |
Reaktionsschritte
To a solution of 4-fluoro-2-methylene-2,3-dihydro-1H-inden-1-one (249b) (3.71 g, 22.9 mmol) and (buta-1,3-dien-2-yloxy)trimethylsilane (5.2 mL, 29.8 mmol) in DCM (200 mL) at 0° C., there was added BF3.Et2O (0.5 mL dropwise. The resulting solution was stirred at 0° C. for another 30 min, quenched with MeOH (0.3 mL), warmed to room temperature, acidified with 2N HCl aqueous solution (15 mL) and extracted with DCM (10 mL×4). The combined organic layers were dried over Na2SO4, filtered and evaporated, and the residue was purified by flash chromatography (0 to 50% EtOAc/Hexane) to give 4′-fluorospiro[cyclohexane-1,2′-indene]-1′,4(3′H)-dione (249c) (2.77 g, 49%). LC-MS tR=1.41 min in 3 min chromatography, MS (ESI) m/z 233 [M+H]+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08633212B2 |
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| Quelldatensatz | uspto-grants-2014_01 |
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| ORD ID | ord-c94d4ddb6dce4f5c957b8a592b55aa4a |
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| Quellennotiz | uspto-grants-2014_01 |
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