Reaktionsgleichung
[Br:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[Cl:9].[N+:10]([O-])([OH:12])=[O:11]>>[Br:1][C:2]1[C:3]([Cl:9])=[CH:4][C:5]([N+:10]([O-:12])=[O:11])=[C:6]([Cl:8])[CH:7]=1Komponenten
3
Versuchsvorschrift
A solution of 2-bromo-1,4-dichlorobenzene (1.000 g, 4.443 mmol, Aldrich, used as received) in fuming HNO3 (7.0 mL) was stirred at 50° C. for 1.5 h and poured into ice (80 g). The yellowish precipitate was filtered, washed with water (10 mL) and dried under vacuum to give 1.14 g (95%) of pure title compound as a yellowish powder; m.p. 50°-53° C.; 1H NMR (CDCl3): 7.863 (s, 1H), 8.030 (s, 1H).
Aufarbeitung
- filtrationThe yellowish precipitate was filtered
- washwashed with water (10 mL)
- customdried under vacuum
Quellen und Nachweise
- ORD-Eintrag
- ord-59b6a6d6fbe44cce97e53977ff3bdff0
- Quelldatensatz
- uspto-grants-1997_04
- Patentnummer
- US05622952
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