Reaktion #94533

ord-89c5e3339af441f5ad92c6c3e237f56e

Reaktionsgleichung

O=C1OC(=O)C(Cl)=C1Cl
2,3-dichloromaleic anhydride
Nc1cccc(C(=O)O)c1C(=O)O
3-aminophthalic acid
O=C1OC(=O)c2c1cccc2N1C(=O)C(Cl)=C(Cl)C1=O
3-(2',3'-dichloromaleinimidyl)-phthalic anhydride
Ausbeute 58.0%

Lösungsmittel

Reaktionsbedingungen

Temperatur
130°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeis produced over the course of approx. 30 minutes
  2. 2
    workup.DISTILLATIONThe dioxane is then distilled off in vacuo (20 mm Hg)
  3. 3
    Temperaturthe crystalline mass is cooled to 50° C.
  4. 4
    workup.ADDITIONmixed with 100 ml of ethyl acetate
  5. 5
    FiltrationThe reaction product is filtered off at 10° C.
  6. 6
    Sonstigedried in vacuo at 80° C

Vorschrift

20 g (0.12 mol) of 2,3-dichloromaleic anhydride are added to a solution of 18.1 g (0.1 mol) of 3-aminophthalic acid in 90 ml of dioxane. The reaction mixture is stirred to 20°-30° C., whereupon a clear solution is produced over the course of approx. 30 minutes. The dioxane is then distilled off in vacuo (20 mm Hg) and the oil which remains is warmed to 130° C. After 3 hours, the crystalline mass is cooled to 50° C. and mixed with 100 ml of ethyl acetate. The reaction product is filtered off at 10° C. and dried in vacuo at 80° C. 18.1 g (58% of theory) of crystalline 3-(2',3'-dichloromaleinimidyl)-phthalic anhydride are obtained, melting at 229°-230° C. after recrystallisation from anhydrous acetic acid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04131613uspto-grants-1978_12