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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 407543Generated: October 29, 2026

m-Chloroperbenzoic acid → 4-Chloro-7-methoxy-8-methylquinoline N-oxide

https://huagongshe.com/reaction/407543

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant4-Chloro-7-methoxy-8-methylquinolineHCID 21101954—
SolventChloroformHCID 6212—
Product4-Chloro-7-methoxy-8-methylquinoline N-oxideHCID 5760794218.3%

Reaction Steps

Metachloroperbenzoic acid (90.2 g, 366.0 mmol) was added portion wise over 3 h to a solution of 4-chloro-7-methoxy-8-methylquinoline (60, 15.2 g, 73.2 mmol) in CHCl3 (1 L). Then, the solution was partitioned between ice-cooled NaOH 1N and CH2Cl2 (8 successive extractions). The organic layers were combined, dried (Na2SO4) and evaporated. The residue was purified by column chromatography (gradient of AcOEt/CH2Cl2, 1:2 to 1:0) to give 3.0 g (18.3%) of the title product 61 as a pale yellow powder: m/z=224 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754106B2
Source datasetuspto-grants-2014_06
ORD IDord-27363d5fa57448b1a431d637b79c3c10
Source noteuspto-grants-2014_06