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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 252013Erstellt: 23. Oktober 2026

Hydrochloric Acid → Ethyl 2-(3-Chloro-2-pyridinyl)-5-oxo-3-pyrazolidinecarboxylate

https://huagongshe.com/de/reaction/252013

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt3-Chloro-2-hydrazinylpyridineHCID 556100—
EduktSodium ethoxideHCID 2723922—
EduktDiethyl MaleateHCID 5271566—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
ProduktEthyl 2-(3-Chloro-2-pyridinyl)-5-oxo-3-pyrazolidinecarboxylateHCID 22280352—

Reaktionsbedingungen

Temperatur65 °C

Reaktionsschritte

To a mixture of 20 g of 3-chloro-2-hydrazinopyridine, 56 ml of sodium ethoxide (a 21% solution in ethanol) and 75 ml of ethanol was added dropwise 27 ml of diethyl maleate. The resulting mixture was heated to reflux for 10 minutes. The reaction mixture was allowed to cool to 65° C., and 15 ml of acetic acid was poured into the mixture. The reaction mixture was allowed to cool to room temperature. After 190 ml of water was poured into the reaction mixture, the mixture was adjusted to pH 2 by an addition of 6N hydrochloric acid and then extracted with methyl tert-butyl ether three times. The organic layers were combined, washed with an aqueous saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. Diethyl ether was added to the resulting residue, and a solid was collected by filtration to obtain 4.28 g of ethyl 2-(3-chloro-2-pyridinyl)-5-oxo-3-pyrazolidinecarboxylate of the formula:

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07867949B2
Quelldatensatzuspto-grants-2011_01
ORD IDord-14f852d1d4f649db8f9598f649336091
Quellennotizuspto-grants-2011_01