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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013689Generated: October 31, 2026

Methanol → HCID 59427334, compound

https://huagongshe.com/reaction/1013689

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 numberUS07981891B2
Source datasetuspto-grants-2011_07
ORD IDord-24a04424d00b4dd6972b48287b6553ef
Source noteuspto-grants-2011_07