Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Allyl iodide | HCID 11166 | — |
| Edukt | 1-Bromo-2-ethylbenzene | HCID 16089 | — |
| Edukt | Magnesium | HCID 5462224 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 3-(2-Ethylphenyl)-1-propene | HCID 18694504 | — |
Reaktionsschritte
To a suspension of 8.53 g (350 mmol) of magnesium in 270 mL of dry THF was added 50 g (270 mmol) of 1-bromo-2-ethyl benzene. The temperature was maintained at 50° C. during addition, then was heated under reflux. After 1 h, the solution was cooled to -78° C. under N2, and 54.42 g (324 mmol) of allyl iodide was added dropwise. The mixture was allowed to warm to room temperature, stirred for an additional 2 h, then cooled to 0° C. The reaction was quenched by addition of 2M HCl and 500 mL of ether and the layers were separated. The organic layer was washed with 30 mL of saturated NaHCO3 solution and brine, dried over MgSO4, filtered and concentrated. The oily residue was filtered through silica gel with 20% ethyl acetate-hexane and the eluate was concentrated to afford the crude 1-allyl-2-ethylbenzene as a colorless oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06051590 |
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| Quelldatensatz | uspto-grants-2000_04 |
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| ORD ID | ord-5fc41e887c3041568b2ae8708bc7e2d7 |
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| Quellennotiz | uspto-grants-2000_04 |
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