HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228618Generated: October 30, 2026
4-Chloro-6,7-dimethoxyquinoline → Ethyl 5-acetyl-2-[(6,7-dimethoxy-4-quinolyl)oxy]benzoate
https://huagongshe.com/reaction/228618
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Chloro-6,7-dimethoxyquinoline | HCID 459610 | — |
| Reactant | Ethyl 5-acetyl-2-hydroxybenzoate | HCID 13408788 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | 1,2-Dichlorobenzene | HCID 7239 | — |
| Product | Ethyl 5-acetyl-2-[(6,7-dimethoxy-4-quinolyl)oxy]benzoate | HCID 57756535 | 9.7% |
Reaction Steps
Ethyl 5-acetylsalicylate (211 mg), 4-chloro-6,7-dimethoxyquinoline (111 mg), and 4-dimethylaminopyridine (183 mg) were suspended in o-dichlorobenzene (1 ml), and the suspension was stirred at 120° C. overnight. The reaction solution was cooled to room temperature, and the solvent was removed by distillation under the reduced pressure. Water was then added to the residue, and the mixture was extracted with chloroform. The chloroform layer was washed with water and was dried over anhydrous sodium sulfate. The solvent was removed therefrom by distillation under the reduced pressure, and the residue was purified by column chromatography using acetone-hexane to give the title compound (19 mg, yield 5%).
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-39fedcec4212456c83d7eb123fdb76cb |
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| Source note | uspto-grants-2009_07 |
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