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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393598Generated: October 29, 2026

7-Benzyloxy-4-chloro-6-methoxyquinoline hydrochloride → 4-Chloro-6-methoxyquinolin-7-ol

https://huagongshe.com/reaction/393598

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Benzyloxy-4-chloro-6-methoxyquinoline hydrochlorideHCID 22646561—
SolventTrifluoroacetic acidHCID 6422—
Product4-Chloro-6-methoxyquinolin-7-olHCID 13558373198%

Reaction Steps

A solution of 7-benzyloxy-4-chloro-6-methoxyquinoline hydrochloride (6.8 g, 20 mmol) in TFA (80 ml) was heated at reflux for 5.5 hours. The volatiles were removed by evaporation, the residue suspended in water and the mixture was adjusted to pH7 with a saturated aqueous sodium hydrogen carbonate solution. The resulting solid was collected by filtration, washed with water, ether and dried under vacuum to give 4-chloro-7-hydroxy-6-methoxyquinoline (4.1 g, 98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06809097B1
Source datasetuspto-grants-2004_10
ORD IDord-a07b263e1f9c44569f87333c7a7d219b
Source noteuspto-grants-2004_10