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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1581489Erstellt: 26. Oktober 2026

Potassium Hydroxide → 6-(2,4-dichloro-phenylsulfanyl)-2H-pyridazin-3-one

https://huagongshe.com/reaction/1581489

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium HydroxideHCID 14797—
Edukt2,4-DichlorobenzenethiolHCID 70730—
Edukt6-Chloropyridazin-3-olHCID 252828—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkt6-(2,4-dichloro-phenylsulfanyl)-2H-pyridazin-3-oneHCID 2250695015,2%

Reaktionsschritte

Potassium t-butoxide (1.1 g) was added to a solution of 2,4-dichlorothiophenol (1.8 g) in N,N-dimethylformamide (DM F) (5 mL). The mixture was stirred at room temperature for 10 minutes and then 6-chloro 2H-pyridazin-3-one (1.31 g) was added. The reaction mixture was stirred at 100° C. for five hours. The mixture was then cooled to room temperature, poured into water (20 mL) and 20% potassium hydroxide (5 mL) was added. The resulting dark solution was extracted with ethyl acetate (2×10 mL). The aqueous layer was collected and the pH was adjusted to 3 with concentrated hydrochloric acid. The solution was then extracted with ethyl acetate (3×10 mL). The ethyl acetate layer was collected, dried over anhydrous sodium sulfate, filtered and evaporated to obtain a crude product, which was purified by silica gel chromatography (1:1 ethyl acetate/hexane as eluent) to afford 6-(2,4-dichloro-phenylsulfanyl)-2H-pyridazin-3-one (418 mg, 15%); NMR 6.88 (d, 1H), 7.10 (d, 1H), 7.24 (dd, 1H), 7.48 (d, 11H), 7.52 (d, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06730674B2
Quelldatensatzuspto-grants-2004_05
ORD IDord-2df3233201634889bffb117900353009
Quellennotizuspto-grants-2004_05