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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452666Generated: October 30, 2026

Dichloromethane → HCID 68663919, compound

https://huagongshe.com/reaction/452666

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 68663323HCID 68663323—
SolventDimethylacetamideHCID 31374—
ProductHCID 68663919HCID 6866391964%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a mixture of 1-[4-(difluoromethoxy)phenyl]-6-[5-(methylthio)-1,3,4-oxadiazol-2-yl]-1H-benzimidazole (3.22 g, 8.60 mmol), dichloromethane (24 mL) and N,N-dimethylacetamide (24 mL) was added m-chloroperbenzoic acid (5.15 g, 21.5 mmol), and the resulting mixture was stirred at 50° C. overnight. 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 silica gel column chromatography (hexane/ethyl acetate=2/1-0/1) and recrystallized from hexane/ethyl acetate to give the title compound (2.23 g, yield 64%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492378B2
Source datasetuspto-grants-2013_07
ORD IDord-468c6799c22249a1b4d08d8dacabf9cb
Source noteuspto-grants-2013_07