Reacción #2006418

ord-88d8d448171c476ca5c56d2592b2845b

Ecuación de reacción

COC(=O)c1ccc(C=CC(=O)c2ccccc2)cc1
enone
COC(=O)c1ccc(C=CC(=O)c2ccccc2)cc1
Methyl-4-(3-oxo-3-phenylpropenyl)-benzoate
CO
MeOH
C[N+]1([O-])CCOCC1
NMO
COC(=O)c1ccc(CCC(=O)c2ccccc2)cc1
Methyl-4-(3-oxo-3-phenylpropyl)-benzoate

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroPurged with nitrogen
  2. 2
    Filtraciónfiltered through Celite
  3. 3
    Otroremoved solvent
  4. 4
    Otroby evaporation under vacuum
  5. 5
    workup.ADDITIONwas added
  6. 6
    workup.STIRRINGStirred at room temperature for 30 minutes
  7. 7
    Filtraciónfiltered through a plug of silica gel
  8. 8
    OtroSolvent was evaporated under vacuum
  9. 9
    Otropurified by column chromatography

Procedimiento

The aromatic enone 46 (321 mg, 1.20 mmol) was dissolved in anhydrous THF (6 mL) and anhydrous MeOH (6 ml). Added 2 small scoops of Pd 10% on activated C, placed under an atmosphere of hydrogen and allowed to stir for 2 hours at room temperature. Purged with nitrogen, filtered through Celite and removed solvent by evaporation under vacuum. The benzylic alcohol is reoxidized to the ketone by the following procedure. The crude was taken back in anhydrous CH2Cl2 (10 mL), with 3 Å molecular sieves, TPAP (1 scoop) was added followed by NMO (212 mg, 1.8 mmol). Stirred at room temperature for 30 minutes and filtered through a plug of silica gel. Solvent was evaporated under vacuum and purified by column chromatography using 10% EtOAc/Hexane.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: USRE043343E1uspto-grants-2012_05