Informations sur le produit
- 1-Azaflavanone
- 2,3-Dihydro-2-phenyl-4-quinolinone derivative
- 2-Phenyl-1,2,3,4-tetrahydro-4-quinolone
- 2-Phenyl-1,2,3,4-tetrahydroquinolin-4-one
- 2-Phenyl-2,3-dihydro-1H-quinolin-4-one
- 4(1H)-Quinolone, 2,3-dihydro-2-phenyl-
- 4(1H)-quinolinone, 2,3-dihydro-2-phenyl-
- Azaflavanone
The synthesis of 2,3-dihydro-2-phenyl-4(1H)-quinolinone is a one-pot reaction that employs a chalcone as the starting material. The chalcone is first converted to an epoxide by using a catalytic amount of acid and then reacted with methoxy in benzene at low temperature. The catalyst is then removed by filtration and the product purified by recrystallization from methanol. This method for synthesizing 2,3-dihydro-2-phenyl-4(1H)-quinolinone is efficient, producing high yields of the desired product.