Reaktion #65892

ord-542d0b8c5cb74239920d2a30bd1d47ab

Reaktionsgleichung

Nc1ccc([N+](=O)[O-])cc1
4-nitroaniline
O=S(Cl)Cl
Thionyl chloride
O=C(O)c1ccccc1Br
2-bromobenzoic acid
O=C(Nc1ccc([N+](=O)[O-])cc1)c1ccccc1Br
2-bromo-N-(4-nitrophenyl)benzamide
Ausbeute 87.0%

Reaktionsbedingungen

Temperatur
80°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe solution was cooled to 20° C.
  2. 2
    Temperaturmaintaining the temperature of the reaction mixture between 20°-25° C
  3. 3
    Sonstigeprecipitated
  4. 4
    workup.ADDITIONWater (360 ml) was added
  5. 5
    workup.STIRRINGwith rigorous stirring
  6. 6
    Filtrationthe suspended solid collected by filtration
  7. 7
    Waschenwashed successively with water, toluene and acetonitrile

Vorschrift

Thionyl chloride (120.5 g) was added to a stirred mixture of 2-bromobenzoic acid (194 g) in toluene (500 ml) and N,N-dimethylformamide (DMF) (5 ml) and the mixture heated at 80° C. for 4 hours. The solution was cooled to 20° C. and added slowly to a solution of 4-nitroaniline (133.1 g) in toluene (500 ml) and NMP (120 ml), maintaining the temperature of the reaction mixture between 20°-25° C. The reaction mixture was then stirred for 24 hours when a solid precipitated. Water (360 ml) was added with rigorous stirring and the suspended solid collected by filtration, and washed successively with water, toluene and acetonitrile to give 2-bromo-N-(4-nitrophenyl)benzamide (B) as a solid, in 87% yield; m.p. 200°-202° C.; NMR(d6 -DMSO): 7.4-7.8(m, 7H), 8.0(d, 2H), 8.3(d, 2H), 11.5(brs, 1H); which was used without further purification.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05420292uspto-grants-1995_05