HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2424278Generated: October 25, 2026
Water → 6-Chloro-3-[2-(methylsulfanyl)phenoxy]pyridazine 1-oxide
https://huagongshe.com/reaction/2424278
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | o-(Methylthio)phenol | HCID 61261 | — |
| Reactant | 3,6-Dichloropyridazine 1-oxide | HCID 260910 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 6-Chloro-3-[2-(methylsulfanyl)phenoxy]pyridazine 1-oxide | HCID 22939933 | 56.8% |
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
| 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-e5fe5966ac024fe8b23104a229d9b802 |
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| Source note | uspto-grants-2011_06 |
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