Reaktionsgleichung
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10]2[NH:14][N:13]=[CH:12][CH:11]=2)=[CH:6][CH:5]=1)([O-:3])=[O:2].[Br:15]N1C(=O)CCC1=O>CN(C)C=O>[Br:15][C:11]1[C:10]([C:7]2[CH:6]=[CH:5][C:4]([N+:1]([O-:3])=[O:2])=[CH:9][CH:8]=2)=[N:14][NH:13][CH:12]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A solution of 5-(4-nitrophenyl)-1H-pyrazole (595 mmol) in N,N-dimethylformamide (1000 mL) was treated with N-bromosuccinimide (654 mmol). The reaction stirred for 30 min at room temperature and was poured into ice-water (1000 mL). Product precipitated out of solution, was filtered, washed with water (4×500 mL) and dried to provide the title product as an off-white powder (90%). ESMS [M+H]+: 269.2
Aufarbeitung
- customProduct precipitated out of solution
- filtrationwas filtered
- washwashed with water (4×500 mL)
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-204a52277c6749b685271428e0447013
- Quelldatensatz
- uspto-grants-2007_10
- Patentnummer
- US07282588B2
Verknüpfte Notizen
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