Reaktion #9848

ord-98cca51794be4ca59ebc9de69d50807e

Reaktionsgleichung

CC(=O)O
acetic acid
Cc1ccccc1[N+](=O)[O-]
2-nitrotoluene
O=c1n(O)c(=O)n(O)c(=O)n1O
hexahydro-1,3,5-trihydroxy-1,3,5-triazine-2,4,6-trione
O=C(O)c1ccccc1[N+](=O)[O-]
2-nitrobenzoic acid
Cc1ccccc1[N+](=O)[O-]
2-nitrotoluene

Lösungsmittel

Reaktionsbedingungen

Temperatur
150°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONThe autoclave was charged with 1 MPa of air
  2. 2
    Sonstigeplaced in a heated oil bath
  3. 3
    SonstigeAfter the completion of reaction
  4. 4
    Temperaturto cool down the reaction mixture quickly

Vorschrift

In an autoclave, 0.274 g of 2-nitrotoluene, 0.018 g of hexahydro-1,3,5-trihydroxy-1,3,5-triazine-2,4,6-trione (5% by mole relative to 2-nitrotoluene), 5 g of acetic acid, 0.003 g of cobalt (II) acetate.4H2O, 0.001 g of manganese(II) acetate.4H2O and 0.018 g of NO2 were placed. The autoclave was charged with 1 MPa of air and placed in a heated oil bath. The mixture was stirred at 150° C. for 14 hours. After the completion of reaction, the autoclave was placed on cold water to cool down the reaction mixture quickly. The resulting mixture was analyzed by gas chromatography and was found to yield 2-nitrobenzoic acid in 62% yield at 67% conversion of 2-nitrotoluene.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07091342B2uspto-grants-2006_08