Acetamide, N-(2-methyl-4-nitrophenyl)- → 2-Methyl-6-nitroaniline

HRID 1534192

Reaktionsgleichung

Reaktionsgleichung von HRID 1534192
C([NH:4][C:5]1[C:10]([N+:11]([O-:13])=[O:12])=[CH:9][CH:8]=[CH:7][C:6]=1[CH3:14])(=O)C.C(NC1C=CC([N+]([O-])=O)=CC=1C)(=O)C>>[NH2:4][C:5]1[C:10]([N+:11]([O-:13])=[O:12])=[CH:9][CH:8]=[CH:7][C:6]=1[CH3:14]

Komponenten

3

Edukt 2

HCID 75936Acetamide, N-(2-methyl-4-nitrophenyl)-HCID 316249N-(2-methyl-6-nitrophenyl)acetamide

Produkt 1

HCID 112982-Methyl-6-nitroanilineAusbeute 46 %

Versuchsvorschrift

The wet mixture of 2-acetylamino-3-nitrotoluene (4) and 2-acetylamino-5-nitrotoluene as obtained in Preparation Example 1 was placed in a steam distillation apparatus, and 300 ml of concentrated hydrochloric acid was added thereto. Immediately on heating and boiling, the mixture was hydrolyzed. The boiling was continued until 36 l of a distillate was collected. On cooling the distillate, there was obtained 2-amino-3-nitrotoluene (5) as an orange needle-like crystal having a melting point of 92.8° to 93.2° C. in a percent yield of 46%.

Aufarbeitung

  1. customas obtained in Preparation Example 1
  2. distillationwas placed in a steam distillation apparatus, and 300 ml of concentrated hydrochloric acid
  3. additionwas added
  4. temperatureImmediately on heating
  5. customwas collected
  6. temperatureOn cooling the distillate, there

Quellen und Nachweise

ORD-Eintrag
ord-e71ff216167e417e8e249f29fb9d1493
Quelldatensatz
uspto-grants-1992_02
Patentnummer
US05087728

Verknüpfte Notizen

Wird geladen…