HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2118826Erstellt: 25. Oktober 2026
Carbon Dioxide → 4-Fluoro-1H-isoindole-1,3(2H)-dione
https://huagongshe.com/reaction/2118826
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Carbon Dioxide | HCID 280 | — |
| Edukt | Urea | HCID 1176 | — |
| Edukt | Sulfolane | HCID 31347 | — |
| Edukt | 3-Fluorophthalic anhydride | HCID 69551 | — |
| Produkt | 4-Fluoro-1H-isoindole-1,3(2H)-dione | HCID 22064632 | — |
Reaktionsschritte
A mixture of 49.8 parts (0.3 mole) of 3-fluorophthalic anhydride and 9.9 parts (0.165 mole) of urea in 126 parts of sulfolane is heated at 125°-130° C., while stirring. The mixture is stirred for 30 minutes, when the evolution of carbon dioxide is complete, after which stirring is continued for a further 15 minutes at 168° C. The solvent is distilled off (98 parts) at a bath temperature of 130°-160° C. under 0.3 mbar. A gas chromatogram shows that it contains 2.75 parts of 3-fluorophthalimide. The distillation residue is triturated with water, and the product is filtered off under suction, washed and dried, 44.5 parts of 3-fluorophthalimide of melting point 179°-182° C. being obtained. The total yield is 47.25 parts (95.3% of theory) of 3-fluorophthalimide.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04680412 |
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| Quelldatensatz | uspto-grants-1987_07 |
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| ORD ID | ord-c31fb8170f8e43ab8d5d16e04e89cdb8 |
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| Quellennotiz | uspto-grants-1987_07 |
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