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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1821662Generated: October 25, 2026

Water → 6-Chloro-3-[2-(methylsulfanyl)phenoxy]pyridazine 1-oxide

https://huagongshe.com/reaction/1821662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactanto-(Methylthio)phenolHCID 61261—
Reactant3,6-Dichloropyridazine 1-oxideHCID 260910—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
Solvent1,4-DioxaneHCID 31275—
Product6-Chloro-3-[2-(methylsulfanyl)phenoxy]pyridazine 1-oxideHCID 2293993356.8%

Reaction Steps

In a mixed solvent of 1,4-dioxane (5 mL) and dimethylsulfoxide (5 mL) was dissolved 454 mg (3.24 mmol) of 2-(methylsulfanyl)phenol, to the solution was added 519 mg (4.63 mmol) of potassium tert-butoxide and the mixture was stirred for 35 minutes. To the mixture was added 424 mg (2.57 mmol) of 3,6-dichloropyridazine 1-oxide and the resulting mixture was stirred for 3 hours. The reaction mixture was poured into water and extracted with ethyl acetate. The organic layers were combined, washed with brine, and dried over anhydrous magnesium sulfate. The solvent was removed, and the obtained residue was purified by silica gel chromatography (Wakogel C-100, eluted with hexane:ethyl acetate=3:1) to obtain 391 mg (1.46 mmol, Yield: 56.8%) of 6-chloro-3-[2-(methylsulfanyl)phenoxy]pyridazine 1-oxide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07608563B2
Source datasetuspto-grants-2009_10
ORD IDord-90620fe223434362948d5aa094bb8a12
Source noteuspto-grants-2009_10