HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1052933Generated: November 1, 2026
Sodium Thiosulfate → HCID 72944738, compound
https://huagongshe.com/reaction/1052933
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 118035230 | HCID 118035230 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 72944738 | HCID 72944738 | — |
Reaction Steps
0.39 g of m-chloroperbenzoic acid (purity of 68%) was added to a mixture of 0.30 g of 2-ethylsulfanyl-N-methyl-N-(5-pentafluoroethyl-pyridin-2-yl)-4-trifluoromethyl-benzamide and 5 mL of chloroform under ice cooling, and the mixture was stirred at room temperature for 2 hours. A saturated aqueous sodium bicarbonate solution and a saturated aqueous sodium thiosulfate solution were added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The resulting residue was applied to a silica gel column chromatography to obtain 0.31 g of 2-ethylsulfonyl-N-methyl-N-(5-pentafluoroethyl-pyridin-2-yl)-4-trifluoromethyl-benzamide (hereinafter, referred to as Compound of Present Invention 9).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09392791B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-4c532c89b4694b8ba521435e6a9af364 |
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| Source note | uspto-grants-2016_07 |
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