Reaktion #95944

ord-d1de302304374230b80adac415af5331

Reaktionsgleichung

NCCNCCN
diethylenetriamine
COC(=O)CC(C)=O
methyl acetoacetate
CCCCCCCCCCCC(=O)O
lauric acid
CCCCCCCCCCCC(=O)NCCN1CCN=C(C)CC1=O
4-lauramidoethyl-7-methyl-3,6-dihydro-2H-1,4-diazepin-5-one

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.DISTILLATIONAt 140° to 150° C., 18 g of water and 32 g of methanol were distilled off
  2. 2
    Sonstigewas effected at 200° to 210° C.
  3. 3
    workup.DISTILLATION18 g of water was distilled off

Vorschrift

Into an apparatus similar to that in Example 1, were charged 103.1 g (1 mole) of diethylenetriamine and 116.1 g (1 mole) of methyl acetoacetate. At 140° to 150° C., 18 g of water and 32 g of methanol were distilled off. Then, with the addition of 200.3 g (1 mole) of lauric acid, the amide formation was effected at 200° to 210° C. and 18 g of water was distilled off, leaving behind 4-lauramidoethyl-7-methyl-3,6-dihydro-2H-1,4-diazepin-5-one.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04346087uspto-grants-1982_08