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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1431308Generated: November 1, 2026

Alumina → 4-Chloro-5,7-difluoro-3-methyl-2-(2-(methylsulfonyl)phenyl)quinoline

https://huagongshe.com/reaction/1431308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAluminaHCID 9989226—
ReactantPotassium hydroxy sulfiteHCID 23707502—
Reactant4-Chloro-5,7-difluoro-3-methyl-2-(2-(methylthio)phenyl)quinolineHCID 59631363—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
Product4-Chloro-5,7-difluoro-3-methyl-2-(2-(methylsulfonyl)phenyl)quinolineHCID 59631037—

Reaction Conditions

Temperature65 °C

Reaction Steps

The 4-chloro-5,7-difluoro-3-methyl-2-(2-(methylthio)phenyl)quinoline (300 mg, 0.893 mmol) was dissolved in chloroform (8 mL) and Oxone™ (1.65 g, 2.68 mmol) and wet aluminum(III) oxide (910 mg, 8.90 mmol) was added. The heterogeneous mixture was stirred vigorously at 65° C. and refluxed for five h. Another portion of Oxone™ (1.65 g, 2.68 mmol) and aluminum(III) oxide (910 mg, 8.90 mmol) was added and the reaction was stirred vigorously overnight at 65° C. The reaction was cooled to rt and slurried in DCM and filtered. The filtrate was concentrated and the crude product was purified by medium pressure chromatography (silica gel, 0 to 50% EtOAc:hexanes) to give 4-chloro-5,7-difluoro-3-methyl-2-(2-(methylsulfonyl)phenyl)quinoline. Mass Spectrum (ESI) m/e=368.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940724B2
Source datasetuspto-grants-2015_01
ORD IDord-2a24eaba3e7440c9874370568e9281c5
Source noteuspto-grants-2015_01