Reacción #75636
ord-76382879dc454d6b9324a56b45a98434
Ecuación de reacción
Reactivos
Ninguno
Condiciones de reacción
Temperatura
-75°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Otroprepared
- 2workup.STIRRINGThe reaction mixture is stirred for 6 hours at −75° C
- 3OtroAfter returning to room temperature
- 4Extracciónextracted with ethyl acetate
- 5OtroThe organic phase is dried
- 6Concentraciónconcentrated
- 7Otropurified 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.