Reaktion #48637

ord-235b4578a1404711aae4882b3e6e9455

Reaktionsgleichung

O=Cc1cc(F)cc(Cl)c1
3-chloro-5-fluorobenzaldehyde
C[N+](=O)[O-]
nitromethane
CC(=O)[O-].[NH4+]
ammonium acetate
O=[N+]([O-])/C=C/c1cc(F)cc(Cl)c1
desired compound
Ausbeute 58.5%
O=[N+]([O-])/C=C/c1cc(F)cc(Cl)c1
1-Chloro-3-fluoro-5-((E)-2-nitrovinyl)-benzene
Ausbeute 58.5%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturto reflux for 4 hours
  2. 2
    TemperaturCool
  3. 3
    workup.ADDITIONpour over ice
  4. 4
    Extraktionextract with ethyl acetate
  5. 5
    Trocknendry (magnesium sulfate)
  6. 6
    Einengenconcentrate
  7. 7
    Sonstigepurify
  8. 8
    Waschen(silica gel chromatography, eluting with 1:1 dichloromethane:hexanes)

Vorschrift

Dissolve 3-chloro-5-fluorobenzaldehyde (4.0 g, 25.2 mmol) in glacial acetic acid (15 mL). Add nitromethane (4.1 mL, 75.7 mmol) and ammonium acetate (1.94 g, 25.2 mmol) and heat to reflux for 4 hours. Cool and pour over ice. Dilute with 2 N sodium hydroxide and extract with ethyl acetate, dry (magnesium sulfate), concentrate and purify (silica gel chromatography, eluting with 1:1 dichloromethane:hexanes) to give the desired compound as a beige solid (2.97 g, 58%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07745438B2uspto-grants-2010_06