Reacción #1435724

ord-ddc6f29da12c4e8aacd3f30c97566c76

Ecuación de reacción

Cl
hydrochloric acid
[H-].[Na+]
sodium hydride
CCOC(=O)CC(=O)OCC
diethyl malonate
Fc1cc(F)c(Br)c(F)c1
1-bromo-2,4,6-trifluorobenzene
CCOC(=O)C(C(=O)OCC)c1c(F)cc(F)cc1F
diethyl (2,4,6-trifluorophenyl)malonate
Rendimiento 43.4%

Condiciones de reacción

Temperatura
40°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONwere added dropwise at room temperature
  2. 2
    Temperaturaunder heating
  3. 3
    Temperaturacooling
  4. 4
    OtroThe organic layer was separated
  5. 5
    Lavadowashed with aqueous sodium hydroxide solution, dil. hydrochloric acid and water subsequently
  6. 6
    Secadodried over sodium sulfate
  7. 7
    Concentraciónconcentrated

Procedimiento

Into a mixture of 4.8 g of sodium hydride (60% in oil) and 100 ml of 1,4-dioxane, 19.2 g of diethyl malonate were added dropwise at room temperature, and then 17.2 g of cuprous bromide and 21.1 g of 1-bromo-2,4,6-trifluorobenzene were subsequently added thereto at 40° C. and refluxed for 26 hours under heating. To the reaction mixture, conc. hydrochloric acid was added under ice-cooling, and then tert-butyl methyl ether and water were added. The organic layer was separated, washed with aqueous sodium hydroxide solution, dil. hydrochloric acid and water subsequently, dried over sodium sulfate and concentrated. The residue was subjected to silica gel column chromatography to give 12.6 g of diethyl (2,4,6-trifluorophenyl)malonate.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07211545B2uspto-grants-2007_05