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Methyl iodide → 2-Bromo-1,3-dimethoxy-5-(1-methoxyethyl)benzene

HRID 41249
ノート
印刷プレビュー

反応式

HRID 41249 の反応式
O1CCC[CH2:2]1.[Br:6][C:7]1[C:12]([O:13][CH3:14])=[CH:11][C:10]([CH:15]([OH:17])[CH3:16])=[CH:9][C:8]=1[O:18][CH3:19].[H-].[Na+].IC>O>[Br:6][C:7]1[C:12]([O:13][CH3:14])=[CH:11][C:10]([CH:15]([O:17][CH3:2])[CH3:16])=[CH:9][C:8]=1[O:18][CH3:19]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 6328Methyl iodideHCID 8028TetrahydrofuranHCID 24758Sodium hydrideHCID 582234841-(4-Bromo-3,5-dimethoxyphenyl)ethanol

生成物 1

HCID 582234192-Bromo-1,3-dimethoxy-5-(1-methoxyethyl)benzene

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

To a tetrahydrofuran (100 mL) solution of 1-(4-bromo-3,5-dimethoxyphenyl)ethanol (7.24 g, 27.7 mmol) was added sodium hydride (1.33 g, 33.2 mmol) at 0° C., and the mixture was stirred for 10 minutes. To the mixture was added dropwise iodomethane (1.90 mL, 30.5 mmol), and the mixture was stirred at room temperature for one hour. After the reaction was completed, water was added to the reaction mixture while cooling on ice, which was extracted with ethyl acetate and dried over anhydrous magnesium sulfate, and the solvent was then distilled off under reduced pressure. The residue was purified by silica gel column chromatography (n-heptane/ethyl acetate: 10/1 then 1/4) to obtain the title compound (7.39 g, 26.9 mmol).

後処理

  1. stirringthe mixture was stirred at room temperature for one hour
  2. temperaturewhile cooling on ice, which
  3. extractionwas extracted with ethyl acetate
  4. dry with materialdried over anhydrous magnesium sulfate
  5. distillationthe solvent was then distilled off under reduced pressure
  6. customThe residue was purified by silica gel column chromatography (n-heptane/ethyl acetate

出典と根拠

ORDレコード
ord-9661cd9f131b4feca1184662d0f3fc1a
出典データセット
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08530504B2

反応ノート

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