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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1821667Generated: October 25, 2026

Water → 6-Chloro-3-(2-methoxy-5-methylphenoxy)pyridazine 1-oxide

https://huagongshe.com/reaction/1821667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-Methoxy-5-methylphenolHCID 14519—
Reactant3,6-Dichloropyridazine 1-oxideHCID 260910—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
Solvent1,4-DioxaneHCID 31275—
Product6-Chloro-3-(2-methoxy-5-methylphenoxy)pyridazine 1-oxideHCID 2294001670.2%

Reaction Steps

In a mixed solvent of 1,4-dioxane (3 mL) and dimethylsulfoxide (3 mL) was dissolved 167.5 mg (1.21 mmol) of commercially available 2-methoxy-5-methylphenol, and 142.8 mg (1.27 mmol) of potassium tert-butoxide was added to the solution, then 202.9 mg (1.23 mmol) of 3,6-dichloropyridazine 1-oxide was added to the mixture and the resulting mixture was stirred at room temperature overnight. The reaction mixture was poured into water, and extracted with ethyl acetate. The organic layer was successively washed with water and 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, 3 plates were used, developed by ethyl acetate:hexane=2:1) to obtain 226.5 mg (0.849 mmol, Yield: 70.2%) of 6-chloro-3-(2-methoxy-5-methylphenoxy)pyridazine 1-oxide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07608563B2
Source datasetuspto-grants-2009_10
ORD IDord-1b8cca4cc3cd466abd35091009dc7e40
Source noteuspto-grants-2009_10