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Imidazole → (2-Bromophenoxy)(tert-butyl)dimethylsilane

HRID 1254268
ノート
印刷プレビュー

反応式

HRID 1254268 の反応式
[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[OH:8].N1C=CN=C1.[Si:14](Cl)([C:17]([CH3:20])([CH3:19])[CH3:18])([CH3:16])[CH3:15].O>CN(C=O)C>[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[O:8][Si:14]([C:17]([CH3:20])([CH3:19])[CH3:18])([CH3:16])[CH3:15]
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 795ImidazoleHCID 962WaterHCID 72442-BromophenolHCID 28928tert-Butyldimethylsilyl chloride

生成物 1

HCID 11219912(2-Bromophenoxy)(tert-butyl)dimethylsilane収率 99.2%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

A solution of 2-bromophenol (5 mL, 47 mmol), imidazole (8 g, 118 mmol) and tert-butyldimethylsilyl chloride (8.6 g, 57 mmol) in DMF (50 mL) was stirred at rt overnight. The reaction was treated with water (150 mL) and extracted with Et2O (4×25 mL). The organic phase was washed with 50% aq lithium chloride solution twice, dried over MgSO4 and filtered. The solvent was evaporated and the crude product was purified by filtration through silica gel, washing with 1:1 EtOAc/hexanes to afford bromo-2-[(tert-butyl)dimethylsiloxy]benzene (13.4 g, 99%).

後処理

  1. extractionextracted with Et2O (4×25 mL)
  2. washThe organic phase was washed with 50% aq lithium chloride solution twice
  3. dry with materialdried over MgSO4
  4. filtrationfiltered
  5. customThe solvent was evaporated
  6. filtrationthe crude product was purified by filtration through silica gel
  7. washwashing with 1:1 EtOAc/hexanes

出典と根拠

ORDレコード
ord-e1ac997f8a3145d5930a5ad85e4a57c9
出典データセット
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08455521B2

反応ノート

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