Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methanol | HCID 887 | — |
| Edukt | 4-Quinolinecarboxylic acid | HCID 10243 | — |
| Edukt | Thionyl Chloride | HCID 24386 | — |
| Produkt | Methyl quinoline-4-carboxylate | HCID 3002895 | 42% |
Reaktionsschritte
Thionyl chloride (4.5 ml) was added dropwise, under argon to a cooled, stirring slurry of 4-quinolinecarboxylic acid (5.32 g) in methanol (120 ml) maintaining an internal temperature of 0 to −5° C. Once addition was complete the reaction mixture was heated at reflux for 16 h. After cooling to ambient temperature the volatiles were removed at reduced pressure and the residue partitioned between saturated aqueous sodium bicarbonate and diethyl ether. The organic phase was washed with brine, dried (Na2SO4) and the solvent removed at reduced pressure to give the title compound as a pale yellow oil (4.82 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06410529B1 |
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| Quelldatensatz | uspto-grants-2002_06 |
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| ORD ID | ord-55adacad8aad49a78e6ae095e2e58d6f |
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| Quellennotiz | uspto-grants-2002_06 |
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