Reaktion #48719

ord-56c0ab958dbe42dcbe4e9c018cf2c7b4

Reaktionsgleichung

O=Cc1cc(F)cc(OCc2ccccc2)c1
3-benzyloxy-5-fluoro-benzaldehyde
C[N+](=O)[O-]
nitromethane
CC(=O)[O-].[NH4+]
ammonium acetate
O=[N+]([O-])/C=C/c1cc(F)cc(OCc2ccccc2)c1
desired compound
Ausbeute 68.5%
O=[N+]([O-])/C=C/c1cc(F)cc(OCc2ccccc2)c1
1-benzyloxy-3-fluoro-5-((E)-2-nitro-vinyl)-benzene
Ausbeute 68.5%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    ExtraktionExtract with hexanes/ethyl acetate
  2. 2
    TrocknenDry (magnesium sulfate)
  3. 3
    Filtrationfilter
  4. 4
    Einengenconcentrate
  5. 5
    SonstigePurify on 120 g silica gel eluting with 100:0 to 80:20 hexanes

Vorschrift

Heat 3-benzyloxy-5-fluoro-benzaldehyde (3.75 g, 16.29 mmol), nitromethane (4.08 g, 66.79 mmol), and ammonium acetate (3.47 g, 44.96 mmol) in acetic acid (54 mL) in 125° C. oil bath under nitrogen for 4 hours. Cool to room temperature and pour into ice/water. Extract with hexanes/ethyl acetate. Dry (magnesium sulfate), filter and concentrate. Purify on 120 g silica gel eluting with 100:0 to 80:20 hexanes:ethyl acetate to give 3.05 g (68.5%) of the desired compound as a yellow oil.

Quelle

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