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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452818Generated: October 30, 2026

Sodium Thiosulfate → HCID 68664042, compound

https://huagongshe.com/reaction/452818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantTriacetoxyperiodinaneHCID 159087—
ReactantHCID 68663489HCID 68663489—
SolventDichloromethaneHCID 6344—
ProductHCID 68664042HCID 6866404257%

Reaction Steps

To a solution of 1-[5-[3-[3-(trifluoromethoxy)phenyl]-1-benzofuran-5-yl]-1,3,4-oxadiazol-2-yl]ethanol (0.30 g, 0.77 mmol) in dichloromethane (3 mL) was added a solution of 1,1,1-triacetoxy-1,1-dihydro-1,2-benziodoxol-3(1H)-one (0.65 g, 1.54 mmol) in dichloromethane (3 mL) at room temperature, and the resulting mixture was stirred overnight. 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 aqueous sodium hydrogen carbonate solution and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=17/3) and recrystallized from hexane/ethyl acetate to give the title compound (0.17 g, yield 57%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492378B2
Source datasetuspto-grants-2013_07
ORD IDord-38049da685b54effab66eb2e58f401b2
Source noteuspto-grants-2013_07