Dimethylformamide → 2-Amino-3-nitrobenzamide
Reaktionsgleichung
[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
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
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
- concentrationThe mixture was concentrated to 300 ml
- additionadded to a mixture of 1500 g of ice and 1500 ml of ammonia
- stirringThe mixture was stirred for 3 h at 5° C
- customThe resulting crystals were isolated at 10° C.
- washwashed with water, 100 ml of iso-propanol, and 100 ml of MTBE
- customdried in a vacuum oven at 50° C
- customRecrystallisation from toluene/MTBE (3/1)
Quellen und Nachweise
- ORD-Eintrag
- ord-a37c5488931e447f901f4e151baa8823
- Quelldatensatz
- uspto-grants-2011_08
- Patentnummer
- US07994160B2
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