Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Diethyl Ether | HCID 3283 | — |
| Edukt | Bromobenzene | HCID 7961 | — |
| Edukt | 2-Chloronicotinonitrile | HCID 81079 | — |
| Edukt | Magnesium | HCID 5462224 | — |
| Produkt | 3-Benzoyl-2-chloropyridine | HCID 824619 | — |
Reaktionsschritte
A solution of 3.14 g (0.02 mols) bromobenzene in anhydrous ether is added dropwise to a suspension of 0.02 mols magnesium in anhydrous ether. The mixture is refluxed 1.5 hr. and is then cooled until room temperature. Now a solution of 1.38 g 2-chloro-3-cyanopyridine in 25 ml anhydrous ether is added slowly while stirring. The reaction mixture is refluxed 24 hrs. and there is added, after standing, 10% aqueous HCl. The aqueous layer is separated and the ethereal layer is washed with 25% aqueous HCl. The combined washings and the first aqueous layer are basified with 40% NaOH and extracted with ether. The combined extracts are dried (MgSO4) and solvent evaporated. The crude is distilled in vacuo. Yield: 0.8 g of title product, identical with that described in Ex. 1b.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04614833 |
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| Quelldatensatz | uspto-grants-1986_09 |
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| ORD ID | ord-da0ee5390b2f4460ba4acde2f5dfb0a5 |
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| Quellennotiz | uspto-grants-1986_09 |
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