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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2193102Generated: October 30, 2026

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

https://huagongshe.com/reaction/2193102

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 numberUS08329694B2
Source datasetuspto-grants-2012_12
ORD IDord-062000aadd0d4ad186eb620fec498592
Source noteuspto-grants-2012_12