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HRID 1821673Erstellt: 26. Oktober 2026

2,6-Dimethylphenol → 6-Chloro-3-(2,6-dimethylphenoxy)pyridazine 1-oxide

https://huagongshe.com/reaction/1821673

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,6-DimethylphenolHCID 11335—
Edukt1,4-DioxaneHCID 31275—
Edukt3,6-Dichloropyridazine 1-oxideHCID 260910—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelDimethyl SulfoxideHCID 679—
Produkt6-Chloro-3-(2,6-dimethylphenoxy)pyridazine 1-oxideHCID 2301380163,2%

Reaktionsschritte

268 mg (2.20 mmol) of 2,6-dimethylphenol, 1,4-dioxane (3 mL) and dimethylsulfoxide (3 mL) were mixed, 270 mg (2.41 mmol) of potassium tert-butoxide was added to the mixture in an ice bath, and the resulting mixture was stirred for 10 minutes. To the mixture was added 370 mg (2.24 mmol) of 3,6-dichloropyridazine 1-oxide, and the resulting mixture was stirred at room temperature for 10 hours and allowed to stand for 2 days. The reaction mixture was poured into ice-cold water, and extracted with ethyl acetate. The organic layers were combined, washed successively with water and brine, and dried over anhydrous sodium sulfate. The solvent was removed, and the residue was purified by silica gel column chromatography (hexane: ethyl acetate, gradient) to obtain 350 mg (1.39 mmol, Yield: 63.1%) of 6-chloro-3-(2,6-dimethylphenoxy)pyridazine 1-oxide.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07608563B2
Quelldatensatzuspto-grants-2009_10
ORD IDord-fb9040a4c4904a93b5f198518a099289
Quellennotizuspto-grants-2009_10