Reaktion #3790

ord-2c2bf9e31bb848cdbaf04402697bce42

Reaktionsgleichung

O=C(O)c1cc([N+](=O)[O-])ccc1Cl
2-chloro-5-nitrobenzoic acid
O=C(Cl)C(=O)Cl
oxalyl chloride
CN(C)C=O
dimethylformamide
NC(=O)c1cc([N+](=O)[O-])ccc1Cl
2-chloro-5-nitro benzamide

Lösungsmittel

Reaktionsbedingungen

Temperatur
0°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 fresh dichloromethane
  3. 3
    Sonstigeammonia was bubbled into the solution for 5 minutes, whereupon the product
  4. 4
    Sonstigeprecipitated from solution
  5. 5
    FiltrationThe product was collected by filtration

Vorschrift

A mixture of 2-chloro-5-nitrobenzoic acid (15.0 g, 74.0 mmol) in 200 mL of dichloromethane was reacted at 24° C. with oxalyl chloride (16.2 mL, 186.0 mmol) and a catalytic amount of dimethylformamide. After 3 hours, the solvent was removed in vacuo, and the residue was redissolved in 200 mL of fresh dichloromethane. The solution was cooled to 0° C., and ammonia was bubbled into the solution for 5 minutes, whereupon the product precipitated from solution. The product was collected by filtration to yield 6.8 g of 2-chloro-5-nitro benzamide, mp 174°-175° C.;

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05734081uspto-grants-1998_03