Reaktion #2028867

ord-b22861604e8e4982808924fed117f64c

Reaktionsgleichung

CC(=O)c1ccc(C)cc1
4′-Methylacetophenone
C[O-].[Na+]
sodium methoxide
CCOC(=O)C(F)(F)F
ethyl trifluoroacetate
Cc1ccc(C(=O)CC(=O)C(F)(F)F)cc1
brown oil
Ausbeute 94.0%
Cc1ccc(C(=O)CC(=O)C(F)(F)F)cc1
1-(4-methylphenyl)-4,4,4-trifluorobutane-1,3-dione
Ausbeute 94.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturAfter refluxing for 24 hours
  2. 2
    Einengenconcentrated
  3. 3
    workup.ADDITION100 mL 10% HCl was added
  4. 4
    Extraktionthe mixture extracted with 4×75 mL ethyl acetate
  5. 5
    TrocknenThe extracts were dried over MgSO4
  6. 6
    Filtrationfiltered
  7. 7
    Einengenconcentrated

Vorschrift

4′-Methylacetophenone (5.26 g, 39.2 mmol) was dissolved in 25 mL of methanol under argon and 12 mL (52.5 mmol) sodium methoxide in methanol (25%) was added. The mixture was stirred for 5 minutes and 5.5 mL (46.2 mmol) ethyl trifluoroacetate was added. After refluxing for 24 hours, the mixture was cooled to room temperature and concentrated. 100 mL 10% HCl was added and the mixture extracted with 4×75 mL ethyl acetate. The extracts were dried over MgSO4, filtered and concentrated to afford 8.47 g (94%) of a brown oil which was carried on without further purification.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: USRE044048E1uspto-grants-2013_03