Acetone → Ethylenebismaleimide

HRID 262419

Reaktionsgleichung

Reaktionsgleichung von HRID 262419
[C:1]1(=[O:7])O[C:4](=[O:5])[CH:3]=[CH:2]1.[CH2:8]([NH2:11])[CH2:9][NH2:10].O.O.O.O.O.O.[Cl-].[Mg+2].[Cl-].C(O[C:25](=[O:27])[CH3:26])(=O)C.[CH3:28][C:29](C)=[O:30]>O.C(N(CC)CC)C>[CH2:8]([N:11]1[C:1](=[O:7])[CH:2]=[CH:3][C:4]1=[O:5])[CH2:9][N:10]1[C:25](=[O:27])[CH:26]=[CH:28][C:29]1=[O:30]

Komponenten

8

Reaktionsbedingungen

Temperatur
40 °C

Versuchsvorschrift

A flask was equipped as in Example 1. To a solution of maleic anhydride (3.64 parts) in 10.6 parts acetone was added a solution of 1 part ethylenediamine, 0.61 part triethylamine and 1.5 parts acetone over a 25-minute period. The resulting reaction mixture contained white solids and was maintained at 40° C. for 30 minutes. Magnesium chloride hexahydrate (0.15 part) and 4.6 parts acetic anhydride were added all at once. The reaction temperature was raised to 50° C. and held there for 2.5 hours. The homogeneous reaction mixture was cooled and 25 parts water added. The precipitated product was filtered by vacuum filtration, washed with water, and dried in a vacuum oven. A 27% yield of N,N'-ethylenedimaleimide, m.p. 193°-194° C., was obtained.

Aufarbeitung

  1. customA flask was equipped as in Example 1
  2. customThe resulting reaction mixture
  3. temperatureThe reaction temperature was raised to 50° C.
  4. temperatureThe homogeneous reaction mixture was cooled
  5. filtrationThe precipitated product was filtered by vacuum filtration
  6. washwashed with water
  7. customdried in a vacuum oven

Quellen und Nachweise

ORD-Eintrag
ord-4e1c03fd2c6f454490ca464d71c987bf
Quelldatensatz
uspto-grants-1979_05
Patentnummer
US04154737

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