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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356716Generated: November 1, 2026

m-Chloroperbenzoic acid → HCID 67548323, compound

https://huagongshe.com/reaction/2356716

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 67547429HCID 67547429—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67548323HCID 6754832378.4%

Reaction Steps

To a solution of 2-(3-fluorophenyl)-5-methylthiomethyl-4-(3-pyridyl)imidazole (152 mg) in tetrahydrofuran (10 ml) was added metachloroperbenzoic acid (97 mg, 70% purity) under ice-cooling, and the mixture was stirred at room temperature for 5 hours. To the reaction mixture was added a saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine and dried over anhydrous sodium sulfate, and the solvent was removed under reduced pressure. The resulting residue was purified by silica gel column chromatography (solvent: chloroform:methanol=19:1), and then, treated with hydrogen chloride-dioxane solution to obtain 2-(3-fluorophenyl)-5-methylsulfinylmethyl-4-(3-pyridyl)imidazole hydrochloride (140 mg) as colorless powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759373B2
Source datasetuspto-grants-2010_07
ORD IDord-ecfae68169a3417a8540c78c127a886d
Source noteuspto-grants-2010_07