Reacción #74882

ord-31ac854078dd47d5a35fc2cb1eaee9ab

Disolventes

Condiciones de reacción

Temperatura
100°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaunder reflux for 1 hour
  2. 2
    OtroIt is then evaporated to dryness in a rotary evaporator
  3. 3
    workup.DISSOLUTIONthe residue is dissolved, at 90° C., in 100 ml of N,N-dimethylacetamide
  4. 4
    TemperaturaAfter cooling
  5. 5
    Filtraciónthe slurry-like mixture is filtered
  6. 6
    Lavadothe residue is rinsed with acetone
  7. 7
    Otrodried in vacuo at 80° C
  8. 8
    OtroIt is then evaporated to dryness
  9. 9
    Otrothe residue is recrystallised from 1,2-dichlorobenzene

Procedimiento

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).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04174326uspto-grants-1979_11