Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-Bromonaphthalene | HCID 7001 | — |
| Edukt | HCID 178418630 | HCID 178418630 | — |
| Katalysator | HCID 178418745 | HCID 178418745 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 1-Cyclopropylnaphthalene | HCID 14668693 | 76% |
Reaktionsschritte
Cyclopropylmagnesium bromide (150 mL, 0.5 M in tetrahydrofuran) was slowly added to a solution of 1-bromo-naphthalene (10 g, 50 mmol) and [1,3-bis(diphenylphosphino)propane]dichloronickel(II) in tetrahydrofuran (10 mL) stirred at 0° C. The reaction mixture was stirred at room temperature for 16 hours and the solvent was evaporated under reduced pressure. EtOAc and ammonium chloride in water were added. After extraction, the organic layer was dried over sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by silica gel chromatography to yield 1-cyclopropyl-naphthalene (6.4 g, 76%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08481581B2 |
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| Quelldatensatz | uspto-grants-2013_07 |
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| ORD ID | ord-ccdd59be48a541a9a605a6921766dcd4 |
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| Quellennotiz | uspto-grants-2013_07 |
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