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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503564Generated: October 30, 2026

Methanol → HCID 59427334, compound

https://huagongshe.com/reaction/503564

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactantm-Chloroperbenzoic acidHCID 70297—
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 numberUS07776857B2
Source datasetuspto-grants-2010_08
ORD IDord-26141a57889741548266fd838f5fee09
Source noteuspto-grants-2010_08