Reacción #1371

ord-2da68ab0871c4a05aa3d4f9224f8df1c

Ecuación de reacción

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
Rendimiento 82.6%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturathe mixture is refluxed for 2.5 hours
  2. 2
    TemperaturaAfter cooling
  3. 3
    Extracciónthe resultant is extracted with diethyl ether
  4. 4
    Secadothe extract is dried over magnesium sulfate
  5. 5
    Concentraciónconcentrated

Procedimiento

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).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05723648uspto-grants-1998_03