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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228870Generated: October 26, 2026

6-(Benzyloxy)-4-chloro-7-methoxyquinoline → 6-Hydroxy-7-methoxyquinoline

https://huagongshe.com/reaction/228870

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-(Benzyloxy)-4-chloro-7-methoxyquinolineHCID 23022781—
CatalystPalladium hydroxideHCID 9942167—
Solventtriethylamine N,N-dimethylformamideHCID 22056947—
Product6-Hydroxy-7-methoxyquinolineHCID 2307842984.1%

Reaction Steps

6-Benzyloxy-4-chloro-7-methoxy-quinoline (525 mg) was dissolved in triethylamine/N,N-dimethylformamide (5 ml/20 ml) to prepare a solution. 20% palladium hydroxide (1.52 g) was added to the solution, and the mixture was stirred at room temperature under a hydrogen gas atmosphere for 6 hr. The reaction solution was filtered, and the solvent was then removed by distillation under the reduced pressure. Water was added to the residue, the mixture was extracted with chloroform, and the chloroform layer was then washed with water and was dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure, and the residue was purified by column chromatography using acetone-chloroform to give 6-hydroxy-7-methoxyquinoline (258 mg, yield 84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560558B2
Source datasetuspto-grants-2009_07
ORD IDord-eb59b987039f4a0c90b72e51d382aaad
Source noteuspto-grants-2009_07