Reacción #2460281

ord-ed3987ac9834488e92847873bef41193

Ecuación de reacción

CCOCC
ether
COCCOCCl
methoxyethoxymethyl chloride
Oc1ccc(I)cc1
4-iodophenol
[H-].[Na+]
sodium hydride
COCCOCOc1ccc(I)cc1
4-Methoxyethoxymethoxy-iodobenzene

Disolventes

Condiciones de reacción

Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturawarmed to room temperature
  2. 2
    workup.STIRRINGstirred for 24 hours
  3. 3
    OtroThe solvent was removed under reduced pressure
  4. 4
    Lavadowashed with 5% sodium hydroxide (4×200 ml), water (4×200 ml), saturated sodium chloride (1×200 ml)
  5. 5
    Secadodried over sodium sulfate
  6. 6
    OtroEvaporation of the solvent under reduced pressure
  7. 7
    Otrogave an oily product in 14.1 g

Procedimiento

A solution of 4-iodophenol (10 g, 45.45 mmol) in 200 ml of anhydrous tetrahydrofuran was treated at 0° C. with sodium hydride (2.36 g, 60% dispersion, 59.09 mmol) for 5 minutes. To the resulting mixture, methoxyethoxymethyl chloride (8.3 ml, 72.73 mmol) was slowly added over a 5-minute period. The mixture was stirred at 0° C. under nitrogen for 30 minutes, warmed to room temperature, and stirred for 24 hours. The solvent was removed under reduced pressure. The residue was taken into 500 ml of ether, washed with 5% sodium hydroxide (4×200 ml), water (4×200 ml), saturated sodium chloride (1×200 ml), and dried over sodium sulfate. Evaporation of the solvent under reduced pressure gave an oily product in 14.1 g. TLC (silica gel, ether): Rf 0.5.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07459284B2uspto-grants-2008_12