HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 54182Erstellt: 23. Oktober 2026
Diethyl 2-(ethoxymethylidene)-3-oxobutanedioate → Triethyl 1,6-dihydro-6-oxo-2,3,5-pyridinetricarboxylate
https://huagongshe.com/de/reaction/54182
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diethyl 2-(ethoxymethylidene)-3-oxobutanedioate | HCID 40590 | — |
| Edukt | Sodium Acetate | HCID 517045 | — |
| Edukt | Ethylmalonamate | HCID 21894451 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | Triethyl 1,6-dihydro-6-oxo-2,3,5-pyridinetricarboxylate | HCID 19958207 | 80,3% |
Reaktionsschritte
A solution of ethylmalonamate (23.6 g, 0.18 mol) in absolute ethanol (300 mL) is added to a stirred solution of diethyl ethoxymethyleneoxalacetate (44.0 g, 0.18 mol) in ethanol (200 mL) at 0° C., followed by the addition, of solid sodium acetate (14.72 g, 0.18 mol). After stirring for ten minutes at 0° C., the mixture is heated to reflux and stirred for 13.5 hours. After cooling, the ethanol is removed under vacuum, and the residue diluted with water and acidified to pH 2 with concentrated hydrochloric acid. The aqueous solution is extracted with methylene chloride (2×200 mL) and the organic layer washed with 300 mL saturated sodium chloride, then dried over anhydrous magnesium sulfate and concentrated in vacuum to give 45.0 g of the title product as an orange oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05622913 |
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| Quelldatensatz | uspto-grants-1997_04 |
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| ORD ID | ord-e115c8113c62468c9cc104c1ac9af4d3 |
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| Quellennotiz | uspto-grants-1997_04 |
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