HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890222Generated: November 2, 2026
Sodium Thiosulfate → HCID 66707627, compound
https://huagongshe.com/reaction/1890222
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 66707627 | HCID 66707627 | — |
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, 205 mg of m-chloroperbenzoic acid was added, followed by stirring at room temperature for 16 hours. To the reaction mixture, an aqueous saturated sodium thiosulfate solution (10 mL) was added, followed by extraction with chloroform (10 mL×2). The organic layer was washed with an aqueous saturated sodium bicarbonate solution (10 mL), dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography (ethyl acetate:hexane=1:1) to obtain 0.23 g of 2,6-dimethyl-5-methylsulfonylmethoxy-4-(2,4,6-triethylphenyl)-3(2H)-pyridazinone [compound (I-4-1)]. Melting point: 142 to 143° C.
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-54626310688541a08c24fc5587a0e3f3 |
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| Source note | uspto-grants-2013_08 |
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