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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 242152Erstellt: 24. Oktober 2026

Ethyl Acetate → (6-Chloropyridazin-3-yl)methanol

https://huagongshe.com/de/reaction/242152

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
EduktThionyl ChlorideHCID 24386—
EduktSodium borohydrideHCID 4311764—
Edukt6-chloropyridazine-3-carboxylic AcidHCID 6415762—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
Produkt(6-Chloropyridazin-3-yl)methanolHCID 20557609—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

4.3 g (21.4 mmol) of 6-chloropyridazine-3-carboxylic acid are dissolved in 60 ml of dry toluene and heated to 60° C. At this temperature, 3.8 g (32.2 mmol) of thionyl chloride are added, and the mixture is stirred at this temperature for 3 h. The mixture is then heated at reflux for 4 h. After cooling to RT, the solvent is removed on a rotary evaporator. 20 ml of toluene are added, and the mixture is again evaporated to dryness. The residue is dissolved in 40 ml of methyl tert-butyl ether and cooled to 5° C. At this temperature, a solution of 1.7 g (47.2 mmol) of sodium borohydride in 37 ml of water is added dropwise. The mixture is stirred at RT for 20 h. 50 ml of ethyl acetate are then added, and the aqueous phase is extracted three times with in each case 10 ml of ethyl acetate. The combined organic phases are washed in each case twice with in each case 10 ml of sat. sodium bicarbonate solution and water. The solvent is removed on a rotary evaporator and the residue is purified chromatographically on silica gel 60 (mobile phase: gradient dichloromethane/ethanol 100:1→20:1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08653109B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-3fd82016978b4fd29e041774b9703100
Quellennotizuspto-grants-2014_02