Reaktion #93765

ord-cac7a746ad3b4282b052d07942965292

Reaktionsgleichung

[Na+].[O-]c1ccccc1
sodium phenoxide
CCC=NO
propionaldehyde oxime
[Na+].[O-]c1ccccc1
sodium phenoxide
CCC(Br)=NO
1-bromo-propionaldehyde oxime
Br
hydrogen bromide
BrBr
bromine
CC(C=NO)Oc1ccccc1
α-phenoxy propionaldehyde oxime

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONintroduced at -5° to 0° C
  2. 2
    FiltrationThe precipitated sodium bromide is collected by filtration
  3. 3
    Einengenthe filtrate concentrated under reduced pressure

Vorschrift

Using the procedure of Example I, propionaldehyde oxime in carbon tetrachloride is brominated with bromine introduced at -5° to 0° C. To the resulting solution of 1-bromo-propionaldehyde oxime is added dropwise with stirring a suspension of sodium phenoxide in carbon tetrachloride. The reaction is allowed to go to completion and any residual sodium phenoxide is neutralized with hydrogen bromide gas. The precipitated sodium bromide is collected by filtration, and the filtrate concentrated under reduced pressure to provide the desired α-phenoxy propionaldehyde oxime.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04614813uspto-grants-1986_09