Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Picolinic acid | HCID 1018 | — |
| Edukt | Diethyl Malonate | HCID 7761 | — |
| Edukt | Cesium carbonate | HCID 10796 | — |
| Edukt | 2-Bromo-5-chloropyridine | HCID 817098 | — |
| Katalysator | HCID 178419072 | HCID 178419072 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | Ethyl 2-(5-chloropyridin-2-YL)acetate | HCID 55263201 | 54% |
Reaktionsschritte
Cesium carbonate (71 g, 218 mmol) was added to 2-bromo-5-chloropyridine (14 g, 73 mmol) and diethyl malonate (22 mL, 145 mmol) in dry 1,4-dioxane (280 mL) and the solution was degassed with argon for 30 minutes. Then copper (I) oxide (2.8 g, 14.55 mmol) and picolinic acid (3.6 g, 29 mmol) were added and the mixture was stirred in a sealed vessel at 130° C. for 24 hours. The mixture was cooled to room temperature, quenched with water (100 mL) and extracted with EtOAc (3×100 ml). The organic extracts were washed with water (200 mL), brine (200 mL), dried over sodium sulfate and evaporated in vacuo. The residue was purified by column chromatography on silica gel (EtOAc:Hexane 92:8) to afford the title compound as a yellow oil in 54% yield, 8.0 g.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08846698B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-81ff80f730b34595aaf541e143b1fa47 |
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| Quellennotiz | uspto-grants-2014_09 |
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