HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 992262Generated: November 1, 2026
Sodium Thiosulfate → HCID 9887398, compound
https://huagongshe.com/reaction/992262
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 9820727 | HCID 9820727 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 9887398 | HCID 9887398 | — |
Reaction Steps
To a solution of 6-acetyl-2-(3-chlorophenyl)-5-methyl-4-phenylthio-3(2H)-pyridazinone (0.37 g) in 1,2-dichloroethane (10 ml) was added m-chloroperbenzoic acid (0.65 g), followed by stirring at room temperature for 12 hours. An aqueous solution of sodium thiosulfate was added to the reaction mixture to decompose excess oxidizing agent, and then the mixture was extracted with chloroform. After washing with a saturated aqueous sodium hydrogen carbonate solution and a brine, the organic layer was dried over anhydrous magnesium sulfate. The solvent was removed by evaporation, and the resulting residue was allowed to stand at room temperature to obtain crystalline 6-acetyl-2-(3-chlorophenyl)-5-methyl-4-phenylsulfonyl-3(2H)-pyridazinone (0.38 g) (Compound No. 1-83).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06469003B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-8a5b4f9e24ec4753a84470b805f3ba45 |
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| Source note | uspto-grants-2002_10 |
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