Reacción #308952

ord-618601587a834845920b5ae396cbdde0

Disolventes

Condiciones de reacción

Temperatura
30°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONwas added to the resultant
  2. 2
    Otroreaction mixture and temperature of the reaction mixture
  3. 3
    OtroReaction mixture
  4. 4
    Extracciónthe crude product was extracted with ethyl acetate (500 mL)
  5. 5
    Lavadoby washing with water, brine
  6. 6
    Secadothe organic layer was dried over anhydrous Na2SO4
  7. 7
    ConcentraciónThe organic layer was concentrated
  8. 8
    Otrothe crude product was purified by column chromatography on silica gel using 4% Ethyl acetate in Hexane

Procedimiento

To an ice cooled solution of 5-bromo-2-fluorobenzaldehyde (10.0 g, 49.2 mmol) in dry DMF (14 mL), Indium powder (8.48 g, 73.7 mmol) was added and stirred for 15 min. ethylbromodifluoroacetate (9.48 ml [14.98 g], 73.7 mmol) in dry DMF (10 mL) was added to the resultant reaction mixture and temperature of the reaction mixture was allowed to warm to rt (30° C.). Stirring continued for 24 h. TLC analysis of the reaction mixture indicated the product formation. Reaction mixture was treated with aqueous saturated NH4Cl solution and the crude product was extracted with ethyl acetate (500 mL) by washing with water, brine and the organic layer was dried over anhydrous Na2SO4. The organic layer was concentrated and the crude product was purified by column chromatography on silica gel using 4% Ethyl acetate in Hexane to obtain title compound as a colorless thick liquid. Yield=12.0 g (75%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08207164B2uspto-grants-2012_06