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Methyl iodide → 7-Methoxy-2-methoxymethylbenzofuran

HRID 2270112
ノート
印刷プレビュー

反応式

HRID 2270112 の反応式
[H-].[Na+].[CH3:3][O:4][C:5]1[C:13]2[O:12][C:11]([CH2:14][OH:15])=[CH:10][C:9]=2[CH:8]=[CH:7][CH:6]=1.I[CH3:17]>O1CCCC1>[CH3:3][O:4][C:5]1[C:13]2[O:12][C:11]([CH2:14][O:15][CH3:17])=[CH:10][C:9]=2[CH:8]=[CH:7][CH:6]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 6328Methyl iodideHCID 24758Sodium hydrideHCID 11788606(7-Methoxy-1-benzofuran-2-yl)methanol

生成物 1

HCID 184236407-Methoxy-2-methoxymethylbenzofuran

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

Sodium hydride (3.82 g, 60% in mineral oil) was added to a solution of 7-methoxy-benzofuran-2-ylmethanol (11.21 g) in dry tetrahydrofuran (300 ml) under an atmosphere of dry nitrogen at room temperature. After 10 minutes iodomethane (15.67 ml) was added and the reaction was left to stir overnight. The solvent was removed in vacuo and the residue partitioned between ethyl acetate (100 ml) and water (50 ml). The organic extract was washed with water (50 ml), followed by brine (50 ml), dried over magnesium sulphate, filtered and the solvent removed in vacuo to afford the title compound (13.32 g) as a yellow oil.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. waitthe reaction was left
  2. customThe solvent was removed in vacuo
  3. customthe residue partitioned between ethyl acetate (100 ml) and water (50 ml)
  4. extractionThe organic extract
  5. washwas washed with water (50 ml)
  6. dry with materialdried over magnesium sulphate
  7. filtrationfiltered
  8. customthe solvent removed in vacuo

出典と根拠

ORDレコード
ord-7bc9e297f1b441f8bebe0ce528e98aa7
出典データセット
uspto-grants-2001_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06331556B2

反応ノート

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