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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 627471Generated: October 31, 2026

6-Bromo-4-hydroxy-3-phenylquinolin-2(1H)-one → 6-Bromo-2-methoxy-3-phenylquinoline

https://huagongshe.com/reaction/627471

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Bromo-4-hydroxy-3-phenylquinolin-2(1H)-oneHCID 86716056—
ReactantHCID 178418582HCID 178418582—
SolventMethanolHCID 887—
Product6-Bromo-2-methoxy-3-phenylquinolineHCID 86716062—

Reaction Steps

In a 100-mL round-bottom flask was placed a mixture of 6-bromo-2-chloro-3-phenylquinoline (550 mg, 1.73 mmol, Intermediate 4, step b) and NaOCH3 (931 mg, 17.2 mmol) in methanol (50 mL). The resulting mixture was refluxed for 5 hours and concentrated under vacuum. The residue was purified by chromatography (silica gel column, 1:5 EtOAc/petroleum ether) to provide the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309222B2
Source datasetuspto-grants-2016_04
ORD IDord-534b53654c2d428db2cc2d91cc7a0a86
Source noteuspto-grants-2016_04