HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890221Generated: November 1, 2026
Sodium Thiosulfate → HCID 66707749, compound
https://huagongshe.com/reaction/1890221
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 66707556 | HCID 66707556 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 66707749 | HCID 66707749 | 95.2% |
Reaction Steps
To a mixture of 0.30 g of 2,6-dimethyl-5-methylthiomethoxy-4-(2,4,6-triethylphenyl)-3(2H)-pyridazinone [compound (I-2-2)] and 4 mL of dichloromethane, 77 mg of m-chloroperbenzoic acid was added, followed by stirring at room temperature for 30 minutes. To the reaction mixture, an aqueous saturated sodium thiosulfate solution (10 mL) was added, followed by extraction with chloroform (10 mL×2). The organic layers was washed with an aqueous saturated sodium bicarbonate solution (10 mL), dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue was subjected to silica gel column chromatography (ethyl acetate) to obtain 0.16 g of 2,6-dimethyl-5-methylsulfinylmethoxy-4-(2,4,6-triethylphenyl)-3(2H)-pyridazinone [compound (I-3-1)].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08507410B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-4a036dbd017d4027bfa6bde9dbb76850 |
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| Source note | uspto-grants-2013_08 |
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