HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452751Generated: November 1, 2026
Sodium Thiosulfate → HCID 68664058, compound
https://huagongshe.com/reaction/452751
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 44482295 | HCID 44482295 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68664058 | HCID 68664058 | 85% |
Reaction Steps
To a solution of 6-(5-methyl-1,3,4-oxadiazol-2-yl)-1-[4-(methylthio)phenyl]-1H-benzimidazole (322 mg, 1.00 mmol) in dichloromethane (10 mL) was added m-chloroperbenzoic acid (479 mg, 2.00 mmol) at 0° C., and the resulting mixture was stirred at room temperature for 1 hr. A saturated aqueous sodium thiosulfate solution was added to the reaction mixture, and the mixture was stirred for 1 hr. The organic layer was separated, washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by basic silica gel column chromatography (hexane/ethyl acetate=4/1-0/1), and recrystallized from hexane/chloroform to give the title compound (302 mg, yield 85%) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08492378B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-db9737aae24d4267b2b77b2dc90abbf9 |
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| Source note | uspto-grants-2013_07 |
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