Benzene, 1-methoxy-3,5-dinitro- → 3,5-Dinitrophenol

HRID 618945Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 618945
[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

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

  1. temperatureto reflux temperature for 16 h
  2. filtrationthe solid precipitate was filtered off
  3. washwashed with water
  4. customdried

Quellen und Nachweise

ORD-Eintrag
ord-db06cdd2ff2a4ae48ebdfc79d58c2b36
Quelldatensatz
uspto-grants-1999_09
Patentnummer
US05958375

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