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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39732Generated: October 25, 2026

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

https://huagongshe.com/reaction/39732

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 numberUS08524738B2
Source datasetuspto-grants-2013_09
ORD IDord-312bddf644ff4e26a162abb45c77c14b
Source noteuspto-grants-2013_09