Diethyl Ether → 4-Methoxyethoxymethoxy-iodobenzene

HRID 2373099

反応式

HRID 2373099 の反応式
[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

参加物

6

反応条件

温度
0 °C

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-ed3987ac9834488e92847873bef41193
出典データセット
uspto-grants-2008_12
特許番号
US07459284B2

関連ノート

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