HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Dimethylformamide → 2-Butenoic acid, 4,4'-(1,3-phenylenediimino)bis(4-oxo-, (2Z,2'Z)-
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Maleic Anhydride | HCID 7923 | — |
| Edukt | M-Phenylenediamine | HCID 7935 | — |
| Edukt | N,N'-1,3-Phenylenedimaleimide | HCID 18156 | — |
| Produkt | 2-Butenoic acid, 4,4'-(1,3-phenylenediimino)bis(4-oxo-, (2Z,2'Z)- | HCID 6436387 | — |
Reaktionsschritte
A typical example of this process is the formation of N,N'-m-phenylenedimaleimide. This involves the addition of maleic anhydride to a solution of m-phenylenediamine in dimethylformamide (DMF) and reacting these at a temperature of 35°-40° C. to form N,N'-m-phenylenedimaleamic acid, which is not isolated. The addition of sodium acetate and acetic anhydride follows, with a maximum reaction temperature for ring closure of 55°-60° C. On the completion of this reaction, a large excess of water is added, precipitating the N,N'-m-phenylenedimaleimide which is subsequently filtered, washed with water, and dried at a moderately elevated temperature. This process is outlined below: ##STR1## N,N'-m-phenylenedimaleimide
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04154737 |
| Quelldatensatz | uspto-grants-1979_05 |
| ORD ID | ord-3f5146fed44841e8a5f378aacd89685a |
| Quellennotiz | uspto-grants-1979_05 |