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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972101Generated: October 26, 2026

8-Hydroxyquinoline → 8-Methoxyquinoline

https://huagongshe.com/reaction/1972101

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-HydroxyquinolineHCID 1923—
ReactantMethyl iodideHCID 6328—
ReactantPotassium HydroxideHCID 14797—
SolventTetrahydrofuranHCID 8028—
Product8-MethoxyquinolineHCID 70310102.4%

Reaction Steps

Add potassium hydroxide (435 g, 7.76 mol) to a solution of 8-hydroxy quinoline (250 g, 1.724 mol) in THF (10 L) at ambient temperature and stir. Add methyl iodide (435 g, 2.58 mol) dropwise and stir overnight. Filter the reaction mixture and wash the solid with THF (2 L). Concentrate the solution to dryness; add water; extract with dichloromethane (2×3 L); combine the organic layers; and wash with brine. Collect the organic layers and dry over sodium sulfate. Remove the solids by filtration. Collect the filtrate and concentrate under reduced pressure to give a red oil, which solidifies on standing, to give the title compound (281 g, 102%), which can be used without further purification. ESI (m/z) 160(M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431706B2
Source datasetuspto-grants-2013_04
ORD IDord-22aff9c0413e4861a47152c17d54eb12
Source noteuspto-grants-2013_04