Diethyl Ether → 4-Methoxyethoxymethoxy-iodobenzene

HRID 1837421

Reaktionsgleichung

Reaktionsgleichung von HRID 1837421
[I:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[CH:4][CH:3]=1.[H-].[Na+].[CH3:11][O:12][CH2:13][CH2:14][O:15][CH2:16]Cl.CCOCC>O1CCCC1>[CH3:11][O:12][CH2:13][CH2:14][O:15][CH2:16][O:8][C:5]1[CH:6]=[CH:7][C:2]([I:1])=[CH:3][CH:4]=1

Komponenten

6

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

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 was slowly added over a 5-minute period methoxyethoxymethyl chloride (8.3 ml, 72.73 mmol). 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 reduce 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.

Aufarbeitung

  1. temperaturewarmed to room temperature
  2. stirringstirred for 24 hours
  3. customThe solvent was removed
  4. washwashed with 5% sodium hydroxide (4×200 ml), water (4×200 ml), saturated sodium chloride (1×200 ml)
  5. dry with materialdried over sodium sulfate
  6. customEvaporation of the solvent under reduced pressure
  7. customgave an oily product in 14.1 g

Quellen und Nachweise

ORD-Eintrag
ord-c362f475903a4840830de9e9c28df0e9
Quelldatensatz
uspto-grants-2004_08
Patentnummer
US06783948B1

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