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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641702Generated: October 31, 2026

m-Chloroperbenzoic acid → HCID 57736544, compound

https://huagongshe.com/reaction/1641702

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 57736435HCID 57736435—
SolventDichloromethaneHCID 6344—
ProductHCID 57736544HCID 5773654419%

Reaction Steps

To a solution of 5-[[(4-fluorophenyl)thio](2,3,6-trifluorophenyl)methyl]-4-m ethylpyridine-2-carboxamide (389 mg, 0.96 mmol) in methylene chloride (10 ml), 3-chloroperbenzoic acid (254 mg, 0.96 mmol) was added at 0° C. After stirring for 13 days at room temperature, the reaction mixture was washed with 1 N aqueous sodium hydroxide. The organic layer was dried over anhydrous sodium sulfate and filtered, then the filtrate was concentrated under reduced pressure, and the resulting residue was subjected to preparative thin-layer chromatography (developed with hexane:ethyl acetate=1:2, eluted with methylene chloride:methanol=4:1). The obtained fraction was concentrated under reduced pressure, and the resulting residue was washed with a mixed solvent of ethanol and diethyl ether, and was collected by filtration, to obtain the title compound (78 mg, 0.18 mmol, 19%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114886B2
Source datasetuspto-grants-2012_02
ORD IDord-3b073a9df5bb4e279e67e677a7f1208a
Source noteuspto-grants-2012_02