Reacción #75636

ord-76382879dc454d6b9324a56b45a98434

Disolventes

Condiciones de reacción

Temperatura
-75°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroprepared
  2. 2
    workup.STIRRINGThe reaction mixture is stirred for 6 hours at −75° C
  3. 3
    OtroAfter returning to room temperature
  4. 4
    Extracciónextracted with ethyl acetate
  5. 5
    OtroThe organic phase is dried
  6. 6
    Concentraciónconcentrated
  7. 7
    Otropurified by chromatography over silica (eluant: cyclohexane/ethyl acetate 8/2)

Procedimiento

27 ml (43.3 mmol) of 1.6M butyllithium in hexane are added, at −75° C., to a solution of 11.4 g (43.3 mmol) of 3-allyl-2-fluoro-4-iodopyridine (prepared according to the process described in J.O.C., 1993, 58, pp. 7832) in 250 ml of THF. After 30 minutes' stirring at −75° C., a solution of 4.6 ml of 3-pentanone in 100 ml of THF is added dropwise. The reaction mixture is stirred for 6 hours at −75° C. After returning to room temperature, the mixture is hydrolysed with 100 ml of water and extracted with ethyl acetate. The organic phase is dried, concentrated and purified by chromatography over silica (eluant: cyclohexane/ethyl acetate 8/2) to yield the expected product.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06699876B2uspto-grants-2004_03