Reacción #1519099

ord-f41363a47ca748ff839e0a6c27866b3a

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 under nitrogen for 24 hours
  3. 3
    OtroThe solvent was removed under reduced pressure
  4. 4
    Lavadowashed with 200 mL of 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 mmoles) in 200 mL of anhydrous tetrahydrofuran was treated at 0° C. with sodium hydride (2.36 g, 60% dispersion, 59.09 mmoles) for 5 minutes. To the resulting mixture was slowly added over a 5 minute period methoxyethoxymethyl chloride (8.3 mL, 72.73 mmoles). The mixture was stirred at 0° C. for 30 minutes, warmed to room temperature, and stirred under nitrogen for 24 hours. The solvent was removed under reduced pressure. The residue was taken into 500 mL of ether, washed with 200 mL of 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: US07611909B1uspto-grants-2009_11