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Imidazole → 1-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]-4-iodobenzene

HRID 341367
ノート
印刷プレビュー

反応式

HRID 341367 の反応式
[I:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[CH:4][CH:3]=1.[Si:9](Cl)([C:12]([CH3:15])([CH3:14])[CH3:13])([CH3:11])[CH3:10].N1C=CN=C1>ClCCl>[C:12]([Si:9]([O:8][C:5]1[CH:6]=[CH:7][C:2]([I:1])=[CH:3][CH:4]=1)([CH3:11])[CH3:10])([CH3:15])([CH3:14])[CH3:13]
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 795ImidazoleHCID 108944-IodophenolHCID 28928tert-Butyldimethylsilyl chloride

生成物 1

HCID 148035271-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]-4-iodobenzene収率 95.3%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

4-Iodophenol (1.0 g, 4.55 mmol) was dissolved in dichloromethane (5 mL). tert-Butyldimethylsilyl chloride (0.685 g, 4.55 mmol) and imidazole (0.309 g, 4.55 mmol) were added. The reaction was stirred overnight at room temperature. The reaction mixture was partitioned between water (30 mL) and dichloromethane (30 mL). The organic layer was removed and the aqueous layer was extracted with dichloromethane (30 mL). The organic layers were combined, dried and concentrated, and the residue was purified by chromatography (0-10% EtOAc/hexanes) to give the title compound as a light yellow oil (1.45 g, 94%).

後処理

  1. customThe reaction mixture was partitioned between water (30 mL) and dichloromethane (30 mL)
  2. customThe organic layer was removed
  3. extractionthe aqueous layer was extracted with dichloromethane (30 mL)
  4. customdried
  5. concentrationconcentrated
  6. customthe residue was purified by chromatography (0-10% EtOAc/hexanes)

出典と根拠

ORDレコード
ord-c267bed69794477a91684b8b46a69e9d
出典データセット
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08895776B2

反応ノート

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