Epichlorohydrin → N-Glycidyl-dimethylmaleimide

HRID 1679096

Reaktionsgleichung

Reaktionsgleichung von HRID 1679096
[CH3:1][C:2]1[C:7](=[O:8])[NH:6][C:4](=[O:5])[C:3]=1[CH3:9].[K].[CH2:11]([CH:13]1[O:15][CH2:14]1)Cl>[Cl-].C[N+](C)(C)C>[CH2:11]([N:6]1[C:7](=[O:8])[C:2]([CH3:1])=[C:3]([CH3:9])[C:4]1=[O:5])[CH:13]1[O:15][CH2:14]1

Komponenten

4

Edukt 2

HCID 7835EpichlorohydrinHCID 70453264Potassium 2,3-dimethylmaleimide

Produkt 1

HCID 20479874N-Glycidyl-dimethylmaleimide

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6379Tetramethylammonium chlorideKatalysator

Versuchsvorschrift

30 g (0.184 mol) of potassium dimethymaleimide are suspended in 175 g (1.89 mols) of epichlorohydrin. After adding 0.05 g of tetramethylammonium chloride, the mixture is heated, whilst stirring, and boiled under reflux for 18 hours and is then filtered. After removing the unconverted chlorohydrin by distillation under a waterpump vacuum, about 30 g of a viscous, pale brown liquid which has an epoxide content of 4.9 equivalents/kg (calculated: 5.5 equivalents/kg) remain. The NMR spectrum of the product corresponds to N-glycidyl-dimethylmaleimide of the formula ##STR31##

Aufarbeitung

  1. temperaturethe mixture is heated
  2. temperatureunder reflux for 18 hours
  3. filtrationis then filtered
  4. customAfter removing the unconverted chlorohydrin
  5. distillationby distillation under a waterpump vacuum, about 30 g of a viscous, pale brown liquid which

Quellen und Nachweise

ORD-Eintrag
ord-750e6b9087b147e7b079a96e930964b3
Quelldatensatz
uspto-grants-1978_03
Patentnummer
US04079041

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