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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1821663Erstellt: 25. Oktober 2026

Sodium Sulfite → 6-Chloro-3-[2-(methylsulfonyl)phenoxy]pyridazine 1-oxide

https://huagongshe.com/reaction/1821663

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium SulfiteHCID 24437—
Eduktm-Chloroperbenzoic acidHCID 70297—
Edukt6-Chloro-3-[2-(methylsulfanyl)phenoxy]pyridazine 1-oxideHCID 22939933—
Lösungsmittel1,2-DichloroethaneHCID 11—
Produkt6-Chloro-3-[2-(methylsulfonyl)phenoxy]pyridazine 1-oxideHCID 2294005056,7%

Reaktionsschritte

In 1,2-dichloroethane (5 mL) was dissolved 208 mg (0.774 mmol) of 6-chloro-3-[2-(methylsulfanyl)phenoxy]pyridazine 1-oxide obtained in Example 11 (1), 829 mg (3.84 mmol) of 80% m-chloroperbenzoic acid was added to the solution and the resulting mixture was stirred at room temperature for 4 hours. The reaction mixture was poured into 10% aqueous sodium sulfite solution, and extracted with ethyl acetate. The organic layers were combined, washed with brine and dried over anhydrous magnesium sulfate. The solvent was distilled off and the obtained residue was purified by preparative thin-layer chromatography (available from Merck Co., 1.05744, developed by hexane:ethyl acetate=1:1) to obtain 132 mg (0.439 mmol, Yield: 56.7%) of 6-chloro-3-[2-(methylsulfonyl)phenoxy]pyridazine 1-oxide.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07608563B2
Quelldatensatzuspto-grants-2009_10
ORD IDord-c3c679b7915647d6aefb22a6a413adf1
Quellennotizuspto-grants-2009_10