Reacción #710490

ord-6943b37c40454913bd5432140eaf993a

Ecuación de reacción

O=P([O-])([O-])[O-].[K+].[K+].[K+]
potassium monophosphate
Clc1cnc(Br)c(Cl)c1
2-bromo-3,5-dichloropyridine
CCOC(=O)C(F)(F)Br
ethyl bromodifluoroacetate
CCOC(=O)C(F)(F)c1ncc(Cl)cc1Cl
brown oil
Rendimiento 86.7%
CCOC(=O)C(F)(F)c1ncc(Cl)cc1Cl
ethyl (3,5-dichloropyridin-2-yl)(difluoro)acetate
Rendimiento 86.7%

Condiciones de reacción

Temperatura
50°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaAfter cooling of the reaction mixture
  2. 2
    FiltraciónThe black mixture was then filtered over a cake of Supercel™
  3. 3
    Lavadothe cake was washed three times by 200 mL of ethyl acetate
  4. 4
    OtroThe organic phases were collected
  5. 5
    Lavadowashed with brine
  6. 6
    Secadodried over magnesium sulfate
  7. 7
    OtroEvaporation of the solvent under vacuum

Procedimiento

To a solution of 56 g (0.246 mol) of 2-bromo-3,5-dichloropyridine in 500 mL of dry dimethylsulfoxide, were added 53 g (0.261 mol) of ethyl bromodifluoroacetate followed by 94 g (0.518 mol) of copper bronze (200 mesh). The beige suspension was heated at 50° C. for 5 hours. After cooling of the reaction mixture, a solution of 44 g (0.328 mol) of potassium monophosphate in 280 mL of water was added and stirred for 1 hour. The black mixture was then filtered over a cake of Supercel™, and the cake was washed three times by 200 mL of ethyl acetate. The organic phases were collected, washed with brine and dried over magnesium sulfate. Evaporation of the solvent under vacuum gave 57.6 g of brown oil. After purification by column chromatography on silica gel (heptane/ethyl acetate 9/1) 40 g (57%) of ethyl (3,5-dichloropyridin-2-yl)(difluoro)acetate (Int-7) were obtained as a yellow oil, (M+1)=270, 19F-NMR (235 MHz, CDCl3) δ (ppm): −104.21 (CF2).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09301526B2uspto-grants-2016_04