Benzene, 1-methoxy-3,5-dinitro- → 3,5-Dinitrophenol
Reaktionsgleichung
[N+:1]([C:4]1[CH:5]=[C:6]([O:13]C)[CH:7]=[C:8]([N+:10]([O-:12])=[O:11])[CH:9]=1)([O-:3])=[O:2]>Br>[N+:1]([C:4]1[CH:5]=[C:6]([OH:13])[CH:7]=[C:8]([N+:10]([O-:12])=[O:11])[CH:9]=1)([O-:3])=[O:2]Komponenten
3
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
3,5-Dinitroanisole (1.36 g, 6.9 mmol) and concentrated aqueous HBr (50 ml) was heated to reflux temperature for 16 h. After cooling to ambient temperature, the solid precipitate was filtered off, washed with water and dried. Yield: 325 mg (26%).
Aufarbeitung
- temperatureto reflux temperature for 16 h
- filtrationthe solid precipitate was filtered off
- washwashed with water
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-db06cdd2ff2a4ae48ebdfc79d58c2b36
- Quelldatensatz
- uspto-grants-1999_09
- Patentnummer
- US05958375
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