HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 478047Erstellt: 24. Oktober 2026
Acetic Anhydride → 1H-Pyrrole-2,5-dione, 1-(3-ethynylphenyl)-
https://huagongshe.com/de/reaction/478047
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Anhydride | HCID 7918 | — |
| Edukt | Maleic Anhydride | HCID 7923 | — |
| Edukt | Benzenamine, 3-ethynyl- | HCID 104682 | — |
| Katalysator | Nickel acetate tetrahydrate | HCID 62601 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 1H-Pyrrole-2,5-dione, 1-(3-ethynylphenyl)- | HCID 710060 | 80,1% |
Reaktionsschritte
Maleic anhydride (79.6 g, 0.81 mole) was added to a solution of distilled 3-aminophenylacetylene (95.1 g, 0.81 mole) dissolved in 500 mL of dry N,N'-dimethylacetamide (DMAc) at 5°-10° C. After addition, another 300 mL of DMAc was added and the mixture stirred at room temperature for two hours. Nickel acetate tetrahydrate (0.8 g) and acetic anhydride (300 mL) were added to the reaction mixture and stirring was continued for 12 hours at room temperature to affect cyclodehydration. The crude product was isolated by precipitation in water and recrystallized from methanol to provide N-(3-ethynylphenyl)maleimide (128 g, 80% yield) as a yellow crystalline solid, mp 129°-131° C. Elemental analysis calculated for C12H7NO2 : C, 73.09%; H, 3.58%; N, 7.10%. Found: C, 72.94%; H, 3.61%; N, 7.04%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04889912 |
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| Quelldatensatz | uspto-grants-1989_12 |
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| ORD ID | ord-c7149af7e208494380914fed1a944b35 |
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| Quellennotiz | uspto-grants-1989_12 |
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