HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228513Generated: October 27, 2026
Water → 2-[(6,7-Dimethoxy-4-quinolyl)oxy]-5-methoxybenzaldehyde
https://huagongshe.com/reaction/228513
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Hydroxy-5-methoxybenzaldehyde | HCID 95695 | — |
| Reactant | 4-Chloro-6,7-dimethoxyquinoline | HCID 459610 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | 2-[(6,7-Dimethoxy-4-quinolyl)oxy]-5-methoxybenzaldehyde | HCID 23078279 | 80.4% |
Reaction Steps
4-Chloro-6,7-dimethoxyquinoline (2.23 g), 2-hydroxy-5-methoxybenzaldehyde (6.08 g), and 4-dimethylaminopyridine (4.88 g) were suspended in monochlorobenzene (40 ml), and the suspension was stirred at 130° C. overnight. The reaction solution was cooled to room temperature, and water was then added thereto. The mixture was extracted with ethyl acetate. The ethyl acetate layer was then washed with water and saturated brine and was dried over anhydrous sodium sulfate. The solvent was removed therefrom by distillation under the reduced pressure, and the residue was purified by chromatography on silica gel using ethyl acetate-hexane for development to give 2-[(6,7-dimethoxy-4-quinolyl)oxy]-5-methoxybenzaldehyde (2.72 g).
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-e85ab466910045919c24bcab69bc2ecd |
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| Source note | uspto-grants-2009_07 |
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