Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 262416Erstellt: 26. Oktober 2026

Acetic Anhydride → N,N'-1,3-Phenylenedimaleimide

https://huagongshe.com/reaction/262416

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AnhydrideHCID 7918—
EduktMaleic AnhydrideHCID 7923—
EduktM-PhenylenediamineHCID 7935—
EduktMagnesium Acetate TetrahydrateHCID 134717—
LösungsmittelAcetoneHCID 180—
LösungsmittelWaterHCID 962—
LösungsmittelTriethylamineHCID 8471—
ProduktN,N'-1,3-PhenylenedimaleimideHCID 1815674%

Reaktionsbedingungen

Temperatur40 °C

Reaktionsschritte

A glass flask was equipped with a thermometer, mechanical paddle stirrer and a water cooled condenser. Crushed maleic anhydride (1.92 parts) was added to a solution of 1 part m-phenylenediamine and 13 parts acetone over a 15-minute period. The heterogeneous reaction mixture was stirred at 40° C. for 1 hour. Acetic anhydride (2.44 parts), 0.32 part triethylamine, and 0.04 part magnesium acetate tetrahydrate were added all at once. The temperature was raised to 60° C. using a heating mantle and maintained for 4 hours. The reaction mixture was cooled, 20 parts water added, and the precipitated product isolated by filtration using a vacuum filter funnel. The filter cake was washed with water and dried for 24 hours at 60°-70° C. in a vacuum oven. A 74% yield of N,N'-m-phenylenedimaleimide, m.p. 203°-204° C. was obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04154737
Quelldatensatzuspto-grants-1979_05
ORD IDord-d49528e09a13439fb3a974f003572bf3
Quellennotizuspto-grants-1979_05