Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2-Chloroquinoline | HCID 11928 | — |
| Edukt | HCID 178419650 | HCID 178419650 | — |
| Katalysator | [1,2-Bis(diphenylphosphino)ethane]dichloronickel(II) | HCID 2734542 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Lösungsmittel | Ammonium Chloride | HCID 25517 | — |
| Produkt | 2-Cyclopentylquinoline | HCID 21826432 | 100,8% |
Reaktionsschritte
To a solution of 2-chloroquinoline (8.2 g, 50 mmol) and [1,2-bis(diphenylphosphino)-ethane]dichloronickel(II) (200 mg, 0.38 mmol) in diethyl ether (20 ml) cooled in a ice/methanol bath was added cyclopentylmagnesium bromide (2 M solution in diethyl ether; 25.5 ml, 51 mmol) over a period of 15 minutes. The resulting brown solution was then stirred for 30 minutes, the ice bath removed and the mixture stirred for a further 10 minutes. The reaction mixture was then re-cooled to 0° C. and a saturated ammonium chloride solution (40 ml) added slowly. The resulting reaction mixture was poured into a separating funnel and further diluted with diethyl ether (60 ml) and saturated ammonium chloride solution (60 ml). The organics were separated and the aqueous layer washed with diethyl ether (2×100 ml). The combined organics were dried (MgSO4), filtered and the solvent removed in vacuo to leave 2-cyclopentylquinoline (9.98 g, 50.4 mmol) as an oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07772227B2 |
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| Quelldatensatz | uspto-grants-2010_08 |
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| ORD ID | ord-6ef299c453e641a5a40b6ddbf30a612a |
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| Quellennotiz | uspto-grants-2010_08 |
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