Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethanol | HCID 702 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 2,5-Dichloro-3-fluoropyridine | HCID 10964877 | — |
| Edukt | HCID 178418416 | HCID 178418416 | — |
| Katalysator | Bis(triphenylphosphine)palladium chloride | HCID 84124 | — |
| Katalysator | HCID 178418476 | HCID 178418476 | — |
| Produkt | Ethyl 5-chloro-3-fluoropicolinate | HCID 22013569 | — |
Reaktionsschritte
An autoclave is charged with 31.4 g of 2,5-dichloro-3-fluoropyridine, 400 ml of dry ethanol, 27.8 ml of triethylamine and 3.5 g of palladium bis(triphenylphosphine) dichloride (PdCl2(PPh3)2) and then a pressure of 180 bars is applied with carbon monoxide. The mixture is maintained at 90° C. for 4 days. After cooling and releasing the pressure, a further 3.5 g of PdCl2(PPh3)2 are added, a pressure of 130 bars is applied with carbon monoxide, and the mixture is maintained at 90° C. for 3 days, after which it is cooled to 25° C., the pressure is released and the mixture is discharged. After concentration in vacuo, absorption from ethyl acetate onto silica gel is carried out. The silica gel is applied to a flash chromatography column (silica gel) and then eluted with n-hexanelethyl acetate 3/1. 24.3 g of the desired target compound having a melting point of 48-50° C. are obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06274536B1 |
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| Quelldatensatz | uspto-grants-2001_08 |
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| ORD ID | ord-060f7c916bff46c7a17eff68139ff51d |
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| Quellennotiz | uspto-grants-2001_08 |
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