Reaktion #1601

ord-119328d4f6c144a381d29ff2f0cd48ad

Reaktionsgleichung

CC(=O)OCc1c2ccccc2c(COC(C)=O)c2ccccc12
acetic
CN(C)C=C(C=O)c1ccc(Cl)cc1
2-(4-chlorophenyl)-3-dimethylaminopropenal
C[O-].[Na+]
sodium methoxide
N#CCC(N)=O
cyanoacetamide
N#Cc1cc(-c2ccc(Cl)cc2)c[nH]c1=O
3-cyano-5-(4-chlorophenyl)-2-pyridinone

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturthe resulting suspension was refluxed overnight
  2. 2
    SonstigeDuring this time a yellow solid was formed
  3. 3
    workup.ADDITIONwas added
  4. 4
    FiltrationThe resulting yellow orange solid was filtered off
  5. 5
    Waschenwashed several times with water
  6. 6
    Sonstigedried

Vorschrift

To solution of sodium methoxide (7.52 g) in methanol (130 ml) was added cyanoacetamide (5.84 g) followed by 2-(4-chlorophenyl)-3-dimethylaminopropenal and the resulting suspension was refluxed overnight. During this time a yellow solid was formed. The mixture was cooled to room temperature and glacial acetic add (50 ml) was added followed by water (100 ml). The resulting yellow orange solid was filtered off, washed several times with water and dried to yield 8.1 g of 3-cyano-5-(4-chlorophenyl)-2-pyridinone.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05726162uspto-grants-1998_03