Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Vinyl Acetate | HCID 7904 | — |
| Edukt | Sodium Carbonate | HCID 10340 | — |
| Edukt | 2-(2-Fluorophenyl)ethan-1-ol | HCID 2733296 | — |
| Katalysator | Chloro(1,5-cyclooctadiene)iridium(I) dimer | HCID 6436381 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 1-Fluoro-2-(2-vinyloxyethyl)-benzene | HCID 68563532 | 72,2% |
Reaktionsschritte
Combine 2-(2-fluorophenyl)-ethanol (3.08 g, 22.0 mmol), vinyl acetate (4 mL, 43.3 mmol), anhydrous toluene (22 mL), chloro(1,5-cyclooctadiene)iridium(I) dimer (155 mg, 0.231 mmol), and anhydrous sodium carbonate (1.5 g, 14.2 mmol) in a dry round-bottom flask fitted with a reflux condensor under a nitrogen atmosphere. Heat the resulting mixture to 95° C. for 5 hours. Cool the reaction mixture to room temperature. Vacuum filter the resultant slurry to remove inorganic precipitates, washing the collected solid with hexanes. Concentrate and purify (silica gel chromatography, eluting with hexanes) to give the title compound as a yellow oil (2.64 g, 72%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07745438B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-7b1b0cb0cdd642c8a96a6098f2f2bb17 |
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| Quellennotiz | uspto-grants-2010_06 |
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