HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444892Generated: October 30, 2026
Sodium Thiosulfate → HCID 86611472, compound
https://huagongshe.com/reaction/1444892
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 86611471 | HCID 86611471 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86611472 | HCID 86611472 | — |
Reaction Steps
In a solution of 0.25 g of 4-[5-(3,5-dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]-2-methylthio-N-(2,2,2-trifluoroethyl)benzoic acid amide (Compound of the present invention No. 5-322) synthesized similarly to Synthetic Example 13 in 6 ml of dichloromethane, 0.17 g of 3-chloroperbenzoic acid was added with stirring at room temperature, and stirred at the same temperature for 3 days. After the completion of the reaction, the reaction mixture was poured in 30 ml of sodium thiosulfate aqueous solution, and extracted with chloroform (10 ml×3). The organic phase was dehydrated with saturated sodium chloride aqueous solution and dried over anhydrous sodium sulfate, and then the solvent was distilled off under reduced pressure. The residue was purified with silica gel column chromatography that was eluated with chloroform, and 0.20 g of the aimed product was obtained as colorless oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07662972B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-d1a5820d864141419cc155d52339c139 |
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| Source note | uspto-grants-2010_02 |
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