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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39730Generated: October 25, 2026

4-Chloro-7-(trifluoromethyl)quinoline → 4-Chloro-1-oxo-7-(trifluoromethyl)-1lambda~5~-quinoline

https://huagongshe.com/reaction/39730

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-7-(trifluoromethyl)quinolineHCID 67668—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
SolventChloroformHCID 6212—
Product4-Chloro-1-oxo-7-(trifluoromethyl)-1lambda~5~-quinolineHCID 23128133—

Reaction Steps

To 14 mL of a chloroform solution containing 0.90 g of 4-chloro-7-trifluoromethylquinoline, 1.04 g of m-chloroperbenzoic acid was added, and the mixture was stirred at room temperature for 3.5 hours. The reaction mixture was added with 15 mL of an aqueous saturated sodium hydrogen carbonate solution. The organic layer was separated, and the aqueous layer was extracted with chloroform. The organic layer and the extract were combined, the resultant solution was washed with an aqueous saturated sodium chloride solution, and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure to obtain a yellow solid, 4-chloro-7-trifluoromethylquinoline N-oxide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524738B2
Source datasetuspto-grants-2013_09
ORD IDord-0c9d7f38499840a9bd74ad95e8a955b4
Source noteuspto-grants-2013_09