Reaktion #2320128

ord-cf9cb58319e1453e9ed7e97945aa2f18

Reaktionsgleichung

[Mg+2].[O-][O-]
magnesium dioxide
CC1CN=C(c2ccccc2)c2ccccc21
1-phenyl-4-methyl-3,4-dihydroisoquinoline
Cc1cnc(-c2ccccc2)c2ccccc12
pure yellow crystals
Ausbeute 42.5%
Cc1cnc(-c2ccccc2)c2ccccc12
1-phenyl-4-methylisoquinoline
Ausbeute 42.5%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe reaction mixture was heated
  2. 2
    Temperaturat reflux for 16 hours
  3. 3
    SonstigeThe magnesium dioxide was removed by vacuum filtration
  4. 4
    Waschenwashed with methylene chloride
  5. 5
    SonstigeEvaporation of the solvent

Vorschrift

To a suspension of activated magnesium dioxide (270 g, 0.132 mol) in 550 mL of benzene was added 1-phenyl-4-methyl-3,4-dihydroisoquinoline (29.0 g, 0.131 mol) with stirring. The reaction mixture was heated at reflux for 16 hours. The magnesium dioxide was removed by vacuum filtration and washed with methylene chloride. Evaporation of the solvent yielded 12.2 g (42%) of pure yellow crystals of 1-phenyl-4-methylisoquinoline.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07709100B2uspto-grants-2010_05