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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2424279Generated: October 25, 2026

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

https://huagongshe.com/reaction/2424279

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium SulfiteHCID 24437—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant6-Chloro-3-[2-(methylsulfanyl)phenoxy]pyridazine 1-oxideHCID 22939933—
Solvent1,2-DichloroethaneHCID 11—
Product6-Chloro-3-[2-(methylsulfonyl)phenoxy]pyridazine 1-oxideHCID 2294005056.7%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07964531B2
Source datasetuspto-grants-2011_06
ORD IDord-571933fd2fb24fb3abb41d1643d1f9b1
Source noteuspto-grants-2011_06