Reaktion #8647

ord-3c966fe269e1451a867618710487421e

Reaktionsgleichung

O=[N+]([O-])c1ccc(N2CCCNCC2)cc1
1-(4-nitrophenyl)[1,4]diazepane
O=C([O-])[O-].[K+].[K+]
potassium carbonate
O=C(Cl)CCl
chloroacetyl chloride
O=C(CCl)N1CCCN(c2ccc([N+](=O)[O-])cc2)CC1
yellow crystals
Ausbeute 75.2%
O=C(CCl)N1CCCN(c2ccc([N+](=O)[O-])cc2)CC1
2-chloro-1-[4-(4-nitrophenyl)[1,4]diazepan-1-yl]ethanone
Ausbeute 75.2%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturwhile maintaining the temperature between 15 and 25° C
  2. 2
    workup.ADDITION400 g of slightly hydrochloric ice-cold water were added to the mixture
  3. 3
    Sonstigea yellow gum crystallized
  4. 4
    FiltrationAfter filtering off by suction
  5. 5
    Waschenwashing with water
  6. 6
    Trocknendrying under vacuum over phosphorus pentoxide

Vorschrift

22.1 g (0.1 mol) of 1-(4-nitrophenyl)[1,4]diazepane, 8.3 g (0.06 mol) of potassium carbonate and 120 ml of dimethylformamide were mixed together in a reactor. 8.3 ml (0.11 mol) of chloroacetyl chloride were added to this stirred suspension, while maintaining the temperature between 15 and 25° C. After stirring for about ten hours at room temperature, 400 g of slightly hydrochloric ice-cold water were added to the mixture: a yellow gum crystallized. After filtering off by suction, washing with water and drying under vacuum over phosphorus pentoxide, 22.4 g of yellow crystals were obtained (yield=75%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07090703B2uspto-grants-2006_08