Reaktion #1371

ord-2da68ab0871c4a05aa3d4f9224f8df1c

Reaktionsgleichung

CCOC(=O)C(C(=O)OCC)C(=O)c1c(F)cc(F)c(F)c1C
diethyl 2-methyl-3,4,6-trifluorobenzoylmalonate
Cc1ccc(S(=O)(=O)O)cc1
p-toluenesulfonic acid
CCOC(=O)CC(=O)c1c(F)cc(F)c(F)c1C
ethyl 2-methyl-3,4,6-trifluorobenzoylacetate
Ausbeute 82.6%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturthe mixture is refluxed for 2.5 hours
  2. 2
    TemperaturAfter cooling
  3. 3
    Extraktionthe resultant is extracted with diethyl ether
  4. 4
    Trocknenthe extract is dried over magnesium sulfate
  5. 5
    Einengenconcentrated

Vorschrift

To diethyl 2-methyl-3,4,6-trifluorobenzoylmalonate (5.1 g) are added water (20 ml) and p-toluenesulfonic acid (30 mg) and the mixture is refluxed for 2.5 hours. After cooling, the resultant is extracted with diethyl ether, and the extract is dried over magnesium sulfate and concentrated to give ethyl 2-methyl-3,4,6-trifluorobenzoylacetate (3.3 g).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05723648uspto-grants-1998_03