Diethyl Ether → 4-Methoxyethoxymethoxy-iodobenzene

HRID 11198

Reaktionsgleichung

Reaktionsgleichung von HRID 11198
[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, 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.

Aufarbeitung

  1. temperaturewarmed to room temperature
  2. stirringstirred for 24 hours
  3. customThe solvent was removed under reduced pressure
  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-3d3933bb35bf467b93b0e9c374f0a8b2
Quelldatensatz
uspto-grants-2006_08
Patentnummer
US07097995B2

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