Reacción #1973930

ord-86e4393017c04939a8fba7c83a118f84

Ecuación de reacción

Cc1ccc(C(NC(=O)c2cccc(C)c2)C(C)O)cc1
N-(2-hydroxy-1-p-tolyl-propyl)-3-methylbezamide
O=[P+3]
phosphorus (V) oxide
C1CCC2CCCCC2C1
decahydronaphtalene
Cc1cccc(-c2ncc(C)c3ccc(C)cc23)c1
1-(3-methylphenyl)-4,7-dimethylisoquinoline

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroAfter completion of the reaction
  2. 2
    Extracciónthe reaction mixture was extracted with dichloromethane and water
  3. 3
    workup.DISTILLATIONdistilled under reduced pressure
  4. 4
    OtroThe resulting residue was purified by silica gel column chromatography
  5. 5
    workup.DISTILLATIONThe eluate was distilled under reduced pressure
  6. 6
    OtroThe residue was recrystallized from dichloromethane and petroleum ether
  7. 7
    Filtraciónfiltered

Procedimiento

N-(2-hydroxy-1-p-tolyl-propyl)-3-methylbezamide (2.1 mmol), phosphorus (V) oxide (10 mmol) and decahydronaphtalene (50 mmol) were put in a dried two-neck round-bottom flask. Then, the mixture was stirred at 120 for 5 hours. After completion of the reaction, the reaction mixture was extracted with dichloromethane and water and distilled under reduced pressure. The resulting residue was purified by silica gel column chromatography. The eluate was distilled under reduced pressure. The residue was recrystallized from dichloromethane and petroleum ether, and filtered to yield 1-(3-methylphenyl)-4,7-dimethylisoquinoline.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08501328B2uspto-grants-2013_08