HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228503Generated: October 29, 2026
Benzaldehyde, 2-hydroxy-5-methyl- → HCID 23078271, compound
https://huagongshe.com/reaction/228503
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzaldehyde, 2-hydroxy-5-methyl- | HCID 69184 | — |
| Reactant | 4-Chloro-6,7-dimethoxyquinoline | HCID 459610 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | 1,2-Dichlorobenzene | HCID 7239 | — |
| Product | HCID 23078271 | HCID 23078271 | 96.1% |
Reaction Steps
4-Chloro-6,7-dimethoxyquinoline (113 mg), 2-hydroxy-5-methylbenzaldehyde (344 mg), and 4-dimethylaminopyridine (313 mg) were suspended in o-dichlorobenzene (5 ml), and the suspension was stirred at 160° C. for 2 hr. The reaction solution was cooled to room temperature, and the solvent was then removed therefrom by distillation under the reduced pressure. Chloroform was added to the residue. The organic layer was washed with a 1 N aqueous sodium hydroxide solution and saturated brine and was dried over anhydrous magnesium sulfate. The solvent was removed therefrom by distillation under the reduced pressure. The residue was purified by column chromatography using chloroform to give the title compound (157 mg, yield 96%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07560558B2 |
|---|
| Source dataset | uspto-grants-2009_07 |
|---|
| ORD ID | ord-c2f1d15658424d48b60144c879dde6f0 |
|---|
| Source note | uspto-grants-2009_07 |
|---|