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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2193104Generated: October 26, 2026

m-Chloroperbenzoic acid → 4-methoxy-7-trifluoromethylquinoline N-oxide

https://huagongshe.com/reaction/2193104

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
Reactant4-methoxy-7-(trifluoromethyl)QuinolineHCID 14513223—
SolventChloroformHCID 6212—
Product4-methoxy-7-trifluoromethylquinoline N-oxideHCID 59398266—

Reaction Steps

To 15 mL of a chloroform solution containing 1.06 g of 4-methoxy-7-trifluoromethylquinoline, 1.36 g of m-chloroperbenzoic acid was added, and the mixture was stirred at room temperature for 16 hours. The reaction mixture was added with 20 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-methoxy-7-trifluoromethylquinoline N-oxide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329694B2
Source datasetuspto-grants-2012_12
ORD IDord-de8570ba6b854f65bfc2407b929a69d6
Source noteuspto-grants-2012_12