Reacción #5088
ord-6ba3ad0efaef42adae43ee53ddb0b4a6
Ecuación de reacción
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1workup.STIRRINGthe whole mixture was stirred at room temperature for 1 hour
- 2Extracciónextracted with 200 ml of methylene chloride
- 3LavadoThe extract was washed with water
- 4Secadodried with anhydrous magnesium sulfate
- 5Concentraciónwas concentrated under a reduced pressure
- 6Otroto obtain the residue
- 7OtroThe residue was recrystallized from ethanol
Procedimiento
Into 15 ml of concentrated sulfuric acid, under ice-cooled condition with stirring, 3.0 g of 2,4-dimethyl-6-(2-phenylacryloyl)phenol was added gradually, then the whole mixture was stirred at room temperature for 1 hour. The reaction mixture was poured in 100 g of ice and extracted with 200 ml of methylene chloride. The extract was washed with water and dried with anhydrous magnesium sulfate, then was concentrated under a reduced pressure to obtain the residue. The residue was recrystallized from ethanol to obtain 2.11 g of 2,3-dihydro-4,6-dimethyl-2-phenyl-7-hydroxy-1H-inden-1-one.