Reacción #336049

ord-de14a4d7a020427c9b58af4c229c58ca

Ecuación de reacción

O=C([O-])O.[Na+]
sodium bicarbonate
Fc1c(F)c(F)c(OC2CCNCC2)c(F)c1F
4-(2,3,4,5,6-pentafluorophenoxy)piperidine
O=CO
formic acid
CC(=O)OCc1c2ccccc2c(COC(C)=O)c2ccccc12
acetic
O=CN1CCC(Oc2c(F)c(F)c(F)c(F)c2F)CC1
1-formyl-4-(2,3,4,5,6-pentafluorophenoxy)piperidine
Rendimiento 91.0%

Condiciones de reacción

Temperatura
55°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturacooled
  2. 2
    workup.STIRRINGThe reaction mixture was then stirred at ambient temperature for three hours
  3. 3
    Extracciónextracted with ethyl acetate
  4. 4
    LavadoThe organic layer was washed with water
  5. 5
    Secadodried over anhydrous magnesium sulfate
  6. 6
    FiltraciónFiltration
  7. 7
    Otrofollowed by evaporation of the solvent
  8. 8
    Otroafforded an oil which
  9. 9
    Otrowas 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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05212184uspto-grants-1993_05