HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 422779Erstellt: 23. Oktober 2026
Methylamine → Ethyl 4-hydroxy-1,2,5-trimethyl-6-oxo-1,6-dihydropyridine-3-carboxylate
https://huagongshe.com/de/reaction/422779
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methylamine | HCID 6329 | — |
| Edukt | 1,1-Diethoxyethene | HCID 137673 | — |
| Edukt | Diethyl 2-methyl-3-oxopentanedioate | HCID 10921903 | — |
| Katalysator | Sodium Methoxide | HCID 10942334 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | Ethyl 4-hydroxy-1,2,5-trimethyl-6-oxo-1,6-dihydropyridine-3-carboxylate | HCID 66673467 | 34% |
Reaktionsschritte
A mixture of 2-methyl-3-oxo-pentanedioic acid diethyl ester (10.0 g, 46.3 mmol), 1,1-diethoxy-ethene (12.8 mL, 92.5 mmol) and sodium methoxide (0.026 mg, 0.481 mmol) was heated to 85° C. for nine hours. The reaction mixture was cooled to room temperature and concentrated. To the resulting residue was added methylamine (1.91 mL, 55.5 mmol, 40% H2O). After stirring at room temperature for 16 hours, the reaction mixture was diluted with diethyl ether and washed with water. The aqueous phase was acidified to pH 1 with 10% HCl solution and extracted with EtOAc. The organic layer was dried (MgSO4) and concentrated. Trituration of the resulting residue with diethyl ether and flash column chromatography (3% MeOH in methylene chloride) gave 3.55 g (34%) desired product.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08101639B2 |
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| Quelldatensatz | uspto-grants-2012_01 |
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| ORD ID | ord-641f7e13a9f343208d3e6d132e3d7ff0 |
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| Quellennotiz | uspto-grants-2012_01 |
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