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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452691Generated: October 30, 2026

Sodium Thiosulfate → HCID 68663351, compound

https://huagongshe.com/reaction/452691

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 68662846HCID 68662846—
SolventAcetonitrileHCID 6342—
ProductHCID 68663351HCID 6866335178%

Reaction Steps

To a solution of 2-(2,3-dihydro-1-benzofuran-5-yl)-5-(methylthio)-1,3,4-oxadiazole (0.50 g, 2.13 mmol) in acetonitrile (10 mL) was added m-chloroperbenzoic acid (70%, 1.51 g, 6.40 mmol) at 0° C., and the obtained mixture was stirred at room temperature for 2 days. A saturated aqueous sodium thiosulfate solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=2/1) to give the title compound (0.44 g, yield 78%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492378B2
Source datasetuspto-grants-2013_07
ORD IDord-78cf6d46426e4ee3ba51b72c90422b03
Source noteuspto-grants-2013_07