Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Carbonate | HCID 10340 | — |
| Edukt | n-Butylamine hydrochloride | HCID 19726 | — |
| Edukt | Sodium Formate | HCID 2723810 | — |
| Edukt | 4-chloro-2-iodo O-crotyl phenol | HCID 69874042 | — |
| Katalysator | palladium(II) acetate | HCID 167845 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 5-Chloro-3-ethyl-benzofuran | HCID 11658384 | 60,4% |
Reaktionsschritte
To a mixture of 4-chloro-2-iodo O-crotyl phenol (1.5 g, 4.86 mmol), sodium carbonate (12.2 mmol, 1.3 g), sodium formate (4.86 mmol, 330 mg), n-butyl ammonium chloride (5.34 mmol, 1.5 g) and DMF (10 mL) was added palladium di-acetate (0.24 mmol, 55 mg). The reaction was heated at 80° C. and maintained at that temperature overnight. After bringing the reaction to room temperature, the mixture was filtered. The filtrate was dried and evaporated to give a crude product, which was purified by silica gel chromatography (eluent: hexanes) to obtain 5-chloro-3-ethyl-benzofuran as a clear oil (60%, 530 mg).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07572910B2 |
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| Quelldatensatz | uspto-grants-2009_08 |
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| ORD ID | ord-260192e041d44e14924799f6057b168a |
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| Quellennotiz | uspto-grants-2009_08 |
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