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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 46604Erstellt: 24. Oktober 2026

Dimethylmaleic anhydride → 3,5-Bis-(dimethylmaleimidyl)-phthalic anhydride

https://huagongshe.com/de/reaction/46604

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylmaleic anhydrideHCID 13010—
EduktDisodium 3,5-diaminophthalateHCID 20346778—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
Produkt3,5-Bis-(dimethylmaleimidyl)-phthalic anhydrideHCID 53973683115,7%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

7.20 g (0.039 mol) of disodium 3,5-diaminophthalate, dissolved in 200 ml of water, are added to a solution of 8.82 g (0.078 mol) of dimethylmaleic anhydride in 80 ml of toluene. This mixture is boiled under reflux for 1 hour. It is then evaporated to dryness in a rotary evaporator, the residue is dissolved, at 90° C., in 100 ml of N,N-dimethylacetamide and 50 ml of water and the solution is rendered acid to Congo Blue with 10% strength hydrochloric acid. After cooling, the slurry-like mixture is filtered and the residue is rinsed with acetone and then dried in vacuo at 80° C. The dry residue is then suspended in 100 ml of acetic anhydride and this mixture is warmed to about 100° C. for 1 hour. It is then evaporated to dryness and the residue is recrystallised from 1,2-dichlorobenzene. 8.9 g (69% of theory) of 3,5-bis-(dimethylmaleimidyl)-phthalic anhydride are obtained; colour: light brownish; melting point 298° C. (decomposition).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04174326
Quelldatensatzuspto-grants-1979_11
ORD IDord-31ac854078dd47d5a35fc2cb1eaee9ab
Quellennotizuspto-grants-1979_11