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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1366753Generated: October 25, 2026

Phenol → 6-Methoxy-7-methyl-1-phenoxyisoquinoline

https://huagongshe.com/reaction/1366753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantPotassium HydroxideHCID 14797—
ReactantSodium HydroxideHCID 14798—
Reactant1-Chloro-6-methoxy-7-methylisoquinolineHCID 53782880—
SolventO-XyleneHCID 7237—
Product6-Methoxy-7-methyl-1-phenoxyisoquinolineHCID 6694178419.6%

Reaction Steps

A mixture of 1-chloro-6-methoxy-7-methyl-isoquinoline (9 g, 43.48 mol), phenol (16.3 g), potassium hydroxide (9.45 g) and xylene (100 ml) was refluxed for 4 days. The reaction mixture was poured out into aqueous sodium hydroxide (4 M) and the xylene layer separated. The aqueous layer was extracted twice with toluene. The combined organic layers were dried (Na2SO4) and concentrated in vacuo to give a residue. The residue was purified by flash chromatography using dichloromethane gave 6-methoxy-7-methyl-1-phenoxyisoquinoline (9 g, 33.96 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893088B2
Source datasetuspto-grants-2011_02
ORD IDord-f69c57d012bd4562b8f92e58c39a4652
Source noteuspto-grants-2011_02