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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl 2-(ethoxymethylidene)-3-oxobutanedioateHCID 40590—
EduktSodium AcetateHCID 517045—
EduktEthylmalonamateHCID 21894451—
LösungsmittelEthanolHCID 702—
ProduktTriethyl 1,6-dihydro-6-oxo-2,3,5-pyridinetricarboxylateHCID 1995820780,3%

Reaktionsbedingungen

Temperatur0 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05622913
Quelldatensatzuspto-grants-1997_04
ORD IDord-e115c8113c62468c9cc104c1ac9af4d3
Quellennotizuspto-grants-1997_04