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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791713Generated: October 30, 2026

Aluminum(III) Chloride → 3-Cyano-7-hydroxyquinoline

https://huagongshe.com/reaction/1791713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant3-Cyano-7-methoxyquinolineHCID 15402200—
SolventBenzeneHCID 241—
Product3-Cyano-7-hydroxyquinolineHCID 13576311768%

Reaction Steps

3-Cyano-7-methoxyquinoline (380 mg, 2.1 mmol) was suspended in benzene (10 ml), aluminium trichloride (826 mg, 6.2 mmol) was added and the mixture heated at reflux for 30 minutes. More aluminium trichloride (275 mg, 2.1 mmol) was added and the mixture refluxed for a further 2 hours. The solvent was evaporated, the dark green solid was added to ice and extracted with ethyl acetate. The organic phase was washed with brine, dried (MgSO4) and evaporated. The solid was found to contain some aluminium salts which were removed as follows. The solid was dissolved in dichloromethane (200 ml) was stirred vigorously with a saturated sodium hydrogen carbonate solution for 1 hour. The product was collected by filtration of the aqueous phase and dried over phosphorus pentoxide under vacuum to give 3-cyano-7-hydroxyquinoline (238 mg, 68%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074800B1
Source datasetuspto-grants-2006_07
ORD IDord-0d77e5cc83ad471fa04f88e630a77a28
Source noteuspto-grants-2006_07