HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452786Generated: October 26, 2026
Sodium Thiosulfate → HCID 68664496, compound
https://huagongshe.com/reaction/452786
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Dimethylacetamide | HCID 31374 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 2-Methyl-5-[3-[4-[2-(methylthio)ethoxy]phenyl]-1-benzofuran-5-yl]-1,3,4-oxadiazole | HCID 68663350 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 68664496 | HCID 68664496 | 27% |
Reaction Steps
To a mixture of 2-methyl-5-[3-[4-[2-(methylthio)ethoxy]phenyl]-1-benzofuran-5-yl]-1,3,4-oxadiazole (186 mg, 0.51 mmol), N,N-dimethylacetamide (2.5 mL) and acetonitrile (2.5 mL) was added m-chloroperbenzoic acid (122 mg, 0.51 mmol) at room temperature, and the resulting mixture was stirred for 2 hr. A saturated aqueous sodium thiosulfate solution was added to the reaction mixture, and the mixture was stirred for 30 min and extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by basic silica gel column chromatography (hexane/ethyl acetate=10/1-0/1) and recrystallized from hexane/ethyl acetate to give the title compound (53.0 mg, yield 27%) 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-0b222b0e4b694ec19504ef51bdb469b0 |
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| Source note | uspto-grants-2013_07 |
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