Dimethylformamide → 2-Amino-3-nitrobenzamide

HRID 1670397Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1670397
[NH2:1][C:2]1[C:10]([N+:11]([O-:13])=[O:12])=[CH:9][CH:8]=[CH:7][C:3]=1[C:4](O)=[O:5].C[N:15](C)C=O.S(Cl)(Cl)=O>O1CCCC1>[NH2:1][C:2]1[C:10]([N+:11]([O-:13])=[O:12])=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([NH2:15])=[O:5]

Komponenten

5

Versuchsvorschrift

To a solution of 100 g (0.55 mol) of acid 5 in 600 ml of tetrahydrofuran (THF) and 1 ml of N,N-dimethylformamide (DMF) 131 g (1.1 mol) of thionyl chloride were added. The mixture was stirred under reflux for 4 h and at room temperature for 12 h. The mixture was concentrated to 300 ml and added to a mixture of 1500 g of ice and 1500 ml of ammonia. The mixture was stirred for 3 h at 5° C. The resulting crystals were isolated at 10° C., washed with water, 100 ml of iso-propanol, and 100 ml of MTBE and dried in a vacuum oven at 50° C. Recrystallisation from toluene/MTBE (3/1). Yield: 68%.

Aufarbeitung

  1. concentrationThe mixture was concentrated to 300 ml
  2. additionadded to a mixture of 1500 g of ice and 1500 ml of ammonia
  3. stirringThe mixture was stirred for 3 h at 5° C
  4. customThe resulting crystals were isolated at 10° C.
  5. washwashed with water, 100 ml of iso-propanol, and 100 ml of MTBE
  6. customdried in a vacuum oven at 50° C
  7. customRecrystallisation from toluene/MTBE (3/1)

Quellen und Nachweise

ORD-Eintrag
ord-a37c5488931e447f901f4e151baa8823
Quelldatensatz
uspto-grants-2011_08
Patentnummer
US07994160B2

Notizen zur Reaktion

Wird geladen…