Reacción #7067

ord-d146ffc4743f46cfb9a96289a70a2846

Ecuación de reacción

COS(=O)(=O)c1ccc(C)cc1
methyl p-toluenesulfonate
CCOC(=O)CC(=O)C(F)(F)F
ethyl 4,4,4-trifluoroacetoacetate
O=C([O-])[O-].[Cs+].[Cs+]
cesium carbonate
CCOC(=O)C=C(OC)C(F)(F)F
title compound
Rendimiento 56.0%
CCOC(=O)C=C(OC)C(F)(F)F
4,4,4-Trifluoro-3-methoxy-but-2-enoic acid ethyl ester
Rendimiento 56.0%

Disolventes

Condiciones de reacción

Temperatura
70°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaAfter cooling to room temperature
  2. 2
    Extracciónextracted with Et2O (2×150 mL)
  3. 3
    Lavadowashed with H2O and brine
  4. 4
    Secadodried (Na2SO4)
  5. 5
    Filtraciónfiltered
  6. 6
    Concentraciónconcentrated

Procedimiento

To a solution of ethyl 4,4,4-trifluoroacetoacetate (12 mL, 82 mmol) in DMF (80 mL) is added cesium carbonate (26.4 g, 82 mmol). The reaction mixture is heated to 70° C. A solution of methyl p-toluenesulfonate (13.5 mL, 90 mmol) in DMF (30 mL) is then added dropwise during 30 min and the reaction mixture is stirred for an additional 1 hr. After cooling to room temperature, the reaction mixture is diluted with H2O (150 mL) and extracted with Et2O (2×150 mL). The organic extracts are combined and washed with H2O and brine, then dried (Na2SO4), filtered and concentrated to afford the title compound (9.0 g, 56%) as an oil which is used without further purification.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07084170B2uspto-grants-2006_08