Reaktion #6489

ord-8a9dfc9e6b4442e382afa28c9f122cb5

Reaktionsgleichung

[K+].[OH-]
potassium hydroxide
O=Cc1cccc(Cl)c1
3-chlorobenzaldehyde
CC(=O)[O-].[NH4+]
ammonium acetate
C[N+](=O)[O-]
nitromethane
O=[N+]([O-])C=Cc1cccc(Cl)c1
title compound
O=[N+]([O-])C=Cc1cccc(Cl)c1
2-(3-Chlorophenyl)-1-nitroethene

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturwas heated
  2. 2
    Temperaturat reflux temperature for 3 h
  3. 3
    workup.ADDITIONpoured onto ice
  4. 4
    FiltrationThe precipitate was filtered
  5. 5
    Sonstigecrystallized from ethyl acetate/hexane

Vorschrift

A mixture of 28.11 g (200 mmol) of 3-chlorobenzaldehyde, 15.4 g of ammonium acetate and 32.5 mL of nitromethane in 230 mL of glacial acetic acid was heated at reflux temperature for 3 h and then poured onto ice. The resultant aqueous mixture was made basic by the addition of 45% aqueous potassium hydroxide. The precipitate was filtered and crystallized from ethyl acetate/hexane to give 5 g of the title compound. The filtrate was concentrated to afford an additional 13.5 g of product.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05248677uspto-grants-1993_09