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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015444Generated: October 31, 2026

m-Chloroperbenzoic acid → HCID 67300738, compound

https://huagongshe.com/reaction/1015444

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 67300467HCID 67300467—
SolventChloroformHCID 6212—
ProductHCID 67300738HCID 67300738—

Reaction Steps

A 300 mg portion of ethyl 1-(4-fluorobenzyl)-2-methyl-3-(methylthio)-1H-indole-5-carboxylate was dissolved in 3 ml of chloroform, and 203 mg of 3-chloroperbenzoic acid was added under ice-cooling, followed by stirring at the same temperature for 1 hour. A saturated sodium bicarbonate aqueous solution was added to the reaction liquid, followed by extraction with ethyl acetate. The organic layer was washed with saturated brine and then dried over anhydrous sodium sulfate. After evaporation of the solvent under a reduced pressure, the residue was purified by silica gel column chromatography (chloroform:methanol:hexane=1:0:1 to 1:0:0 to 100:1:0 to 50:1:0 to 30:1:0) to obtain 279 mg of ethyl 1-(4-fluorobenzyl)-2-methyl-3-(methylsulfinyl)-1H-indole-5-carboxylate as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985764B2
Source datasetuspto-grants-2011_07
ORD IDord-9ede6a0996824d1ba5e4d97172b6bd60
Source noteuspto-grants-2011_07