Reacción #5088

ord-6ba3ad0efaef42adae43ee53ddb0b4a6

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.STIRRINGthe whole mixture was stirred at room temperature for 1 hour
  2. 2
    Extracciónextracted with 200 ml of methylene chloride
  3. 3
    LavadoThe extract was washed with water
  4. 4
    Secadodried with anhydrous magnesium sulfate
  5. 5
    Concentraciónwas concentrated under a reduced pressure
  6. 6
    Otroto obtain the residue
  7. 7
    OtroThe 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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05242919uspto-grants-1993_09