반응 #2006418

ord-88d8d448171c476ca5c56d2592b2845b

반응 방정식

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

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타Purged with nitrogen
  2. 2
    여과filtered through Celite
  3. 3
    기타removed solvent
  4. 4
    기타by evaporation under vacuum
  5. 5
    workup.ADDITIONwas added
  6. 6
    workup.STIRRINGStirred at room temperature for 30 minutes
  7. 7
    여과filtered through a plug of silica gel
  8. 8
    기타Solvent was evaporated under vacuum
  9. 9
    기타purified by column chromatography

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: USRE043343E1uspto-grants-2012_05