Reaktion #2028884

ord-86e9ef1581f54ccbaf93858808191b56

Reaktionsgleichung

Cl
HCl
C[O-].[Na+]
sodium methoxide
CCOC(=O)C(F)(F)F
Ethyl trifluoroacetate
Cc1ccc2c(c1)CCCC2=O
6-methyltetralone
Cc1ccc2c(c1)CCC(C(=O)C(F)(F)F)C2=O
oil
Ausbeute 85.1%
Cc1ccc2c(c1)CCC(C(=O)C(F)(F)F)C2=O
6-methyl-2-(trifluoroacetyl)tetralone
Ausbeute 85.1%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe organic layer was collected
  2. 2
    Waschenwashed with brine
  3. 3
    Trocknendried over MgSO4
  4. 4
    Einengenconcentrated in vacuo

Vorschrift

Ethyl trifluoroacetate (5.33 g, 37.5 mmol) was dissolved in ether (50 mL) and treated with a sodium methoxide solution (25% in methanol, 9.92 g, 45.9 mmol) followed by 6-methyltetralone (5.94 g, 37.1 mmol). The reaction was stirred at room temperature for 6.1 hours then treated with 1N HCl (20 mL). The organic layer was collected, washed with brine, dried over MgSO4, and concentrated in vacuo to give a brown oil (8.09 g) that was used in the next step without further purification.

Quelle

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