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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1717289Erstellt: 26. Oktober 2026

Sodium ethoxide → HCID 68515561, Verbindung

https://huagongshe.com/reaction/1717289

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium ethoxideHCID 2723922—
EduktEthyl 5-methyl-3-oxohex-4-enoateHCID 15564232—
Edukt4-azido-N-ethylbenzamideHCID 59432226—
LösungsmittelEthanolHCID 702—
ProduktHCID 68515561HCID 6851556178,2%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

Ethyl 5-methyl-3-oxo-4-hexenoate (1.10 g, 6.56 mmol, 1.1 eq.) obtained in Example 95a) and 4-azido-N-ethylbenzamide (purity 90%, 1.23 g, 5.82 mmol) were dissolved in ethanol (25 ml), sodium ethoxide (550 mg, 7.82 mmol, 1.25 eq.) was added, and the mixture was stirred at room temperature for 30 min and at 50° C. for 10.5 hr. Ethanol was evaporated from the reaction mixture, and the residue was diluted with 2% aqueous sodium carbonate solution (40 ml) and washed with ethyl acetate (40 ml). The organic layer was extracted with 2% aqueous sodium carbonate solution (15 ml). The aqueous layers were combined, washed with ethyl acetate-hexane (2:1, 50 ml), acidified (pH<3) with 6N hydrochloric acid and extracted three times with ethyl acetate (50 ml) and ethyl acetate-THF (3:1, 40 ml). The organic layers were combined, washed with saturated brine, dried over anhydrous sodium sulfate and concentrated, and ethyl acetate was added. The precipitate was collected by filtration, washed with ethyl acetate and diethyl ether and dried to give the title compound as a grayish white powder (1.43 g, 4.55 mmol, 78.2%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07803822B2
Quelldatensatzuspto-grants-2010_09
ORD IDord-b87e60d71d604214bc6a8beced7c9519
Quellennotizuspto-grants-2010_09