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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375769Generated: October 31, 2026

Methanesulfonic Acid → 4-Chloro-6-methoxyquinolin-7-ol

https://huagongshe.com/reaction/1375769

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantThioanisoleHCID 7520—
Reactant7-(Benzyloxy)-4-chloro-6-methoxyquinolineHCID 22646562—
SolventTrifluoromethanesulfonic acidHCID 62406—
Product4-Chloro-6-methoxyquinolin-7-olHCID 13558373175.8%

Reaction Steps

7-(Benzyloxy)-4-chloro-6-methoxyquinoline (100 mg), thioanisole (300 μl), and methanesulfonic acid (25 μl) were dissolved in trifluoromethanesulfonic acid (1 ml). The solution was stirred at room temperature for 30 min. The solvent was removed by distillation under the reduced pressure. The residue was made neutral by the addition of an aqueous sodium hydroxide solution, and hexane was added thereto to prepare a suspension. The crystal was collected by suction filtration to give 53 mg (yield 75%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07169789B2
Source datasetuspto-grants-2007_01
ORD IDord-8664bd8bc62a48d0bac85bc1ae2fc2b3
Source noteuspto-grants-2007_01