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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Homophthalic anhydride | HCID 12801 | — |
| Reactant | 4-Methoxybenzylamine | HCID 75452 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(4-Methoxy-benzyl)-4H-isoquinoline-1,3-dione | HCID 1475552 | 84% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06583144B2 |
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| Source dataset | uspto-grants-2003_06 |
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| ORD ID | ord-786fdc14e398476285a2f5a47195429a |
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| Source note | uspto-grants-2003_06 |
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