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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 6-Chloro-3-[2-(methylsulfanyl)phenoxy]pyridazine 1-oxide | HCID 22939933 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 6-Chloro-3-[2-(methylsulfonyl)phenoxy]pyridazine 1-oxide | HCID 22940050 | 56.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07964531B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-571933fd2fb24fb3abb41d1643d1f9b1 |
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| Source note | uspto-grants-2011_06 |
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