Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Chloride | HCID 312 | — |
| Edukt | 4-Fluorobenzyl chloride | HCID 9602 | — |
| Edukt | 1H-Indene, 2-bromo- | HCID 575586 | — |
| Edukt | Magnesium | HCID 5462224 | — |
| Katalysator | HCID 178418745 | HCID 178418745 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | 2-(4-Fluorophenylmethyl)indene | HCID 21976997 | — |
Reaktionsschritte
To a suspension of freshly ground magnesium (0.58 g, 23 mmol) in 100 mL of ether was added about 3 mL of a 15 mL ether solution containing 3.0 g (21 mmol) of 4-fluorophenylmethyl chloride. The system was carefully heated and after initiation of the reaction, the remaining chloride solution added over 30 minutes while maintain a gentle reflux. After refluxing for 1.5 hours, the Grignard solution was cooled and cannulated to a mixture of 3.65 g (19 mmol) of 2-bromo-indene, 150 mg (0.20 mmol) of NiCl2(dppp) and 100 mL of ether. The system was gently heated to reflux overnight and then cooled and quenched by adding 150 mL of 1.0 M aqueous hydrochloric acid. The product was isolated and purified (hexanes/silica) as for 2-benzyl-indene. Yield: 3.45 g, 74 percent
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07098356B2 |
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| Quelldatensatz | uspto-grants-2006_08 |
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| ORD ID | ord-c95ea336c63e4d4ea8961bed6584d030 |
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| Quellennotiz | uspto-grants-2006_08 |
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