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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042829Generated: October 28, 2026

Methanol → HCID 59427334, compound

https://huagongshe.com/reaction/1042829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 59598389HCID 59598389—
SolventDichloromethaneHCID 6344—
ProductHCID 59427334HCID 5942733494%

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 CH2Cl2 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 (1.37 g, 94% yield) as a off-white foam. MH+=284.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557816B2
Source datasetuspto-grants-2013_10
ORD IDord-8257882e2bc545a2a2578b6078157ea5
Source noteuspto-grants-2013_10