تفاعل #2006418

ord-88d8d448171c476ca5c56d2592b2845b

معادلة التفاعل

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

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىPurged with nitrogen
  2. 2
    ترشيحfiltered through Celite
  3. 3
    أخرىremoved solvent
  4. 4
    أخرىby evaporation under vacuum
  5. 5
    workup.ADDITIONwas added
  6. 6
    workup.STIRRINGStirred at room temperature for 30 minutes
  7. 7
    ترشيحfiltered through a plug of silica gel
  8. 8
    أخرىSolvent was evaporated under vacuum
  9. 9
    أخرىpurified by column chromatography

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: USRE043343E1uspto-grants-2012_05