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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1370568Generated: October 30, 2026

Homophthalic anhydride → 2-(4-Methoxy-benzyl)-4H-isoquinoline-1,3-dione

https://huagongshe.com/reaction/1370568

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHomophthalic anhydrideHCID 12801—
Reactant4-MethoxybenzylamineHCID 75452—
SolventWaterHCID 962—
Product2-(4-Methoxy-benzyl)-4H-isoquinoline-1,3-dioneHCID 147555284%

Reaction Conditions

Temperature180 °C

Reaction Steps

4-Methoxybenzylamine (8.3 g) was added to homophthalic anhydride (8.1 g). The mixture was stirred at 180° C. overnight. Water was added to the reaction solution. The mixture was then extracted with ethyl acetate. The organic layer was then dried over anhydrous magnesium sulfate. The solvent was removed by distillation under the reduced pressure. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate=8:2) to give 2-(4-methoxybenzyl)-4H-isoquinoline-1,3-dione (11.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06583144B2
Source datasetuspto-grants-2003_06
ORD IDord-786fdc14e398476285a2f5a47195429a
Source noteuspto-grants-2003_06