HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228611Generated: October 27, 2026
Ethyl 5-chlorosalicylate → Ethyl 5-chloro-2-[(6,7-dimethoxy-4-quinolyl)oxy]benzoate
https://huagongshe.com/reaction/228611
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 5-chlorosalicylate | HCID 306053 | — |
| Reactant | 4-Chloro-6,7-dimethoxyquinoline | HCID 459610 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | 1,2-Dichlorobenzene | HCID 7239 | — |
| Product | Ethyl 5-chloro-2-[(6,7-dimethoxy-4-quinolyl)oxy]benzoate | HCID 57756520 | 15% |
Reaction Steps
Ethyl 5-chlorosalicylate (147 mg), 4-chloro-6,7-dimethoxyquinoline (165 mg), and 4-dimethylaminopyridine (270 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 (41 mg, yield 15%).
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-edc9593703514545813f03fa943052e4 |
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| Source note | uspto-grants-2009_07 |
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