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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 6-(Benzyloxy)-4-chloro-7-methoxyquinoline | HCID 23022781 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | triethylamine N,N-dimethylformamide | HCID 22056947 | — |
| Product | 6-Hydroxy-7-methoxyquinoline | HCID 23078429 | 84.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07560558B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-eb59b987039f4a0c90b72e51d382aaad |
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| Source note | uspto-grants-2009_07 |
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