Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehyde, 2-hydroxy-5-methyl-HCID 69184—
Reactant4-Chloro-6,7-dimethoxyquinolineHCID 459610—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
Solvent1,2-DichlorobenzeneHCID 7239—
ProductHCID 23078271HCID 2307827196.1%

Reaction Conditions

Temperature160 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560558B2
Source datasetuspto-grants-2009_07
ORD IDord-c2f1d15658424d48b60144c879dde6f0
Source noteuspto-grants-2009_07