Réaction #2460281

ord-ed3987ac9834488e92847873bef41193

Équation de réaction

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

Conditions de réaction

Température
0°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températurewarmed to room temperature
  2. 2
    workup.STIRRINGstirred for 24 hours
  3. 3
    AutreThe solvent was removed under reduced pressure
  4. 4
    Lavagewashed with 5% sodium hydroxide (4×200 ml), water (4×200 ml), saturated sodium chloride (1×200 ml)
  5. 5
    Séchagedried over sodium sulfate
  6. 6
    AutreEvaporation of the solvent under reduced pressure
  7. 7
    Autregave an oily product in 14.1 g

Mode opératoire

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07459284B2uspto-grants-2008_12