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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042875Generated: October 31, 2026

m-Chloroperbenzoic acid → HCID 59427334, compound

https://huagongshe.com/reaction/1042875

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 59598389HCID 59598389—
SolventDichloromethaneHCID 6344—
ProductHCID 59427334HCID 59427334—

Reaction Steps

To 7-methoxy-4-(phenylthio)quinoline (1.38 g, 5.16 mmol) in CH2Cl2 (50 mL) at −78° C. was added m-CPBA (77%) (1.25 g, 7.23 mmol) portionwise. The mixture was allowed to slowly warm to RT (3 hrs). The reaction mixture was diluted with CH2Cl2 then neutralized with NaHCO3 (sat.). The aqueous phase was extracted three times with DCM then the organic layer was dried over Na2SO4, filtered, and concentrated in vacuo. The crude mixture was purified by silica gel chromatography using 0-10% CH2Cl2:MeOH to afford 7-methoxy-4-(phenylsulfinyl)quinoline as a off-white foam. MS: M+H+=284.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557816B2
Source datasetuspto-grants-2013_10
ORD IDord-bf8f623d99334852b7cc0a8a62b562ef
Source noteuspto-grants-2013_10