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HRID 1244255Erstellt: 24. Oktober 2026

Hydrochloric Acid → 6-Chloro-4-ethoxy-pyridazine-3-carboxylic acid ethyl ester

https://huagongshe.com/de/reaction/1244255

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSodium BicarbonateHCID 516892—
EduktSodium ethoxideHCID 2723922—
EduktEthyl 4,6-dichloropyridazine-3-carboxylateHCID 53428795—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produkt6-Chloro-4-ethoxy-pyridazine-3-carboxylic acid ethyl esterHCID 85961304—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Sodium ethoxide (1.16 g, 17 mmol) is added to a stirred solution of 4,6-dichloropyridazine-3-carboxylic acid ethyl ester (3.73 g, 17 mmol) in THF (45 mL) cooled to 0° C. The reaction mixture is stirred at room temperature overnight and then poured into 1N HCl (20 mL). The resulting solution is then neutralized with saturated NaHCO3. EtOAc (20 mL) is added and the layers are separated. The aqueous layer is extracted twice with EtOAc (20 mL) and the combined extracts are washed with brine (25 mL), dried (Na2SO4), and evaporated. The residue is then purified by flash column chromatography (silica gel, eluted with 2:1 Hexane, EtOAc) to give the title product as a white solid. H1 NMR δ (CDCl3) 7.02 (s, 1H), 4.47 (q, 2H, J=7.2 Hz), 4.19 (q, 2H, J=7.2 Hz), 1.50 (t, 3H, J=7.2 Hz), 1.41 (t, 3H, J=7.2 Hz).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07122546B2
Quelldatensatzuspto-grants-2006_10
ORD IDord-368648d478334543afe2f74ff5c032db
Quellennotizuspto-grants-2006_10