Reacción #336049
ord-de14a4d7a020427c9b58af4c229c58ca
Ecuación de reacción
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1Temperaturacooled
- 2workup.STIRRINGThe reaction mixture was then stirred at ambient temperature for three hours
- 3Extracciónextracted with ethyl acetate
- 4LavadoThe organic layer was washed with water
- 5Secadodried over anhydrous magnesium sulfate
- 6FiltraciónFiltration
- 7Otrofollowed by evaporation of the solvent
- 8Otroafforded an oil which
- 9Otrowas purified by means of high pressure liquid chromatography (silica gel; elution with ethyl acetate)
Procedimiento
A mixture of 1.5 ml of formic acid and 3.5 ml of acetic anydride was stirred at 55° C. for one hour, cooled, and treated with a solution of 4.0 g of 4-(2,3,4,5,6-pentafluorophenoxy)piperidine in 50 ml of diethyl ether. The reaction mixture was then stirred at ambient temperature for three hours. Thereafter, the mixture was poured into 100 ml of water, adjusted to pH 10 by the addition of sodium bicarbonate, and extracted with ethyl acetate. The organic layer was washed with water followed by a saturated solution of chloride and dried over anhydrous magnesium sulfate. Filtration, followed by evaporation of the solvent afforded an oil which was purified by means of high pressure liquid chromatography (silica gel; elution with ethyl acetate) to yield 4.0 g (91%) of 1-formyl-4-(2,3,4,5,6-pentafluorophenoxy)piperidine, m.p. 32°-34° C.