Reaktion #3353

ord-669072172d11414b8d8b946fb369fa91

Reaktionsgleichung

CN(C)C=O
dimethylformamide
O=C(O)c1cc([N+](=O)[O-])ccc1Cl
2-chloro-5-nitrobenzoic acid
ClCCl
dichloromethane
O=C(Cl)C(=O)Cl
oxalyl chloride
NC(=O)c1cc([N+](=O)[O-])ccc1Cl
2-Chloro-5-nitrobenzamide

Reaktionsbedingungen

Temperatur
25°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe solvent was removed in vacuo
  2. 2
    workup.DISSOLUTIONthe residue was redissolved in 200 mL of dichloromethane
  3. 3
    TemperaturThe solution was cooled to 0° C.
  4. 4
    Sonstigeammonia was bubbled through the cold solution for 5 minutes, whereupon the product
  5. 5
    Sonstigeprecipitated
  6. 6
    Sonstigeto form solution
  7. 7
    FiltrationThe product was collected by filtration
  8. 8
    Sonstigeto yield 6.8 g, mp 174°-175° C.

Vorschrift

A mixture of 2-chloro-5-nitrobenzoic acid (15.0 g, 74.0 mmol) and 200 mL of dichloromethane was reacted with oxalyl chloride (16.2 mL, 186.0 mmol) and a catalytic amount of dimethylformamide. The mixture was stirred at 25° C. for 3 hours. The solvent was removed in vacuo, and the residue was redissolved in 200 mL of dichloromethane. The solution was cooled to 0° C., and ammonia was bubbled through the cold solution for 5 minutes, whereupon the product precipitated to form solution. The product was collected by filtration to yield 6.8 g, mp 174°-175° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05733921uspto-grants-1998_03