Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509339Generated: October 25, 2026

m-Chloroperbenzoic acid → Methyl quinoline-6-carboxylate 1-oxide

https://huagongshe.com/reaction/509339

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantMethyl quinoline-6-carboxylateHCID 736812—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
ProductMethyl quinoline-6-carboxylate 1-oxideHCID 21707072—

Reaction Steps

To a solution of methyl quinoline-6-carboxylate from above in DCM (10 mL) was added 3-chlorobenzoperoxoic acid (1.991 g, 11.54 mmol). The reaction was stirred 21 h at rt. The mixture was then diluted with saturated aqueous NaHCO3 (40 mL), and the mixture was extracted with DCM (2×30 mL). The organic layers were combined, washed with saturated aqueous NaCl (40 mL), dried (MgSO4), and concentrated. The N-oxide was isolated as an orange solid which was used without purification in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096527B2
Source datasetuspto-grants-2015_08
ORD IDord-0efa6437beea438190ece568991c95c4
Source noteuspto-grants-2015_08