HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713649Generated: November 2, 2026
Sodium Thiosulfate → HCID 118113340, compound
https://huagongshe.com/reaction/713649
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 118113456 | HCID 118113456 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 118113340 | HCID 118113340 | — |
Reaction Steps
1.15 g of m-chloroperbenzoic acid (purity of 68%) was added to a mixture of 0.78 g of 3-ethylsulfanyl-N-(3,5-bistrifluoromethylphenyl)picolinamide (Compound of Present Invention 10) and 10 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 poured to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and then concentrated under reduced pressure, and the resulting solid was washed with MTBE and dried to obtain 0.78 g of 3-ethylsulfonyl-N-(3,5-bistrifluoromethylphenyl)picolinamide (hereinafter, referred to as Compound of Present Invention 14).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09185910B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-3782407c8e324d679b7b8c408bd548e6 |
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| Source note | uspto-grants-2015_11 |
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