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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AnhydrideHCID 7918—
EduktMaleic AnhydrideHCID 7923—
EduktBenzenamine, 3-ethynyl-HCID 104682—
KatalysatorNickel acetate tetrahydrateHCID 62601—
LösungsmittelWaterHCID 962—
Produkt1H-Pyrrole-2,5-dione, 1-(3-ethynylphenyl)-HCID 71006080,1%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04889912
Quelldatensatzuspto-grants-1989_12
ORD IDord-c7149af7e208494380914fed1a944b35
Quellennotizuspto-grants-1989_12