Acetone → 4-Benzyl-1,4,7,10-tetraazacyclododecane-2,6-dione

HRID 1488359Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1488359
C[CH:2]([N:6]([CH:14](C)[C:15]([O-:17])=O)[CH2:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[C:3]([O-:5])=O.[NH2:19][CH2:20][CH2:21][NH:22][CH2:23][CH2:24][NH2:25].CC(C)=O>C(O)C>[CH2:7]([N:6]1[CH2:2][C:3](=[O:5])[NH:25][CH2:24][CH2:23][NH:22][CH2:21][CH2:20][NH:19][C:15](=[O:17])[CH2:14]1)[C:8]1[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=1

Komponenten

5

Edukt 3

HCID 180AcetoneHCID 8111DiethylenetriamineHCID 131719217dimethyl-N-benzyl-iminodiacetate

Produkt 1

HCID 157028294-Benzyl-1,4,7,10-tetraazacyclododecane-2,6-dioneAusbeute 14,4 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel2×

Versuchsvorschrift

To a solution of 31.2 g dimethyl-N-benzyliminodiacetate in 2.5 l of dry ethanol at reflux under nitrogen was added dropwise 12.8 g of di-ethylenetriamine in 160 ml of dry ethanol. Reflux was carried out for a total of 137 hours. The solution was evaporated under reduced pressure leaving a yellow paste. Trituration with acetone left 5.2 g of the desired product as a colorless solid.

Aufarbeitung

  1. temperatureReflux
  2. customwas carried out for a total of 137 hours
  3. customThe solution was evaporated under reduced pressure
  4. customleaving a yellow paste

Quellen und Nachweise

ORD-Eintrag
ord-3b14d40eed40422db39b7643abc6da76
Quelldatensatz
uspto-grants-1997_10
Patentnummer
US05674470

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