Reacción #828780
ord-66d45603f05d409fbf714dcf6827df2b
Ecuación de reacción
Reactivos
Ninguno
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Temperaturathe resulting suspension was refluxed overnight
- 2OtroDuring this time a yellow solid was formed
- 3FiltraciónThe resulting yellow orange solid was filtered off
- 4Lavadowashed several times with water
- 5Otrodried
Procedimiento
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 acid (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.