Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2370781Generated: October 26, 2026

m-Chloroperbenzoic acid → 7-(Methoxycarbonyl)quinoline 1-oxide

https://huagongshe.com/reaction/2370781

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantMethyl quinoline-7-carboxylateHCID 12554532—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
Product7-(Methoxycarbonyl)quinoline 1-oxideHCID 67491695—

Reaction Steps

To a solution of the methyl quinoline-7-carboxylate from above in DCM (10 mL) was added 3-chlorobenzoperoxoic acid (1.991 g, 11.54 mmol). The reaction was stirred for 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 numberUS08710043B2
Source datasetuspto-grants-2014_04
ORD IDord-23e7bbd846d44e01aef7bfe95fab0e30
Source noteuspto-grants-2014_04