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Imidazole → (4-Bromo-3-isopropyl-phenoxy)-tert-butyl-dimethyl-silane

HRID 278795
ノート
印刷プレビュー

反応式

HRID 278795 の反応式
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[CH:4][C:3]=1[CH:9]([CH3:11])[CH3:10].Cl[Si:13]([C:16]([CH3:19])([CH3:18])[CH3:17])([CH3:15])[CH3:14].N1C=CN=C1>CN(C=O)C.O>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][Si:13]([C:16]([CH3:19])([CH3:18])[CH3:17])([CH3:15])[CH3:14])=[CH:4][C:3]=1[CH:9]([CH3:11])[CH3:10]
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 3

HCID 795ImidazoleHCID 28928tert-Butyldimethylsilyl chlorideHCID 225688014-Bromo-3-isopropylphenol2 回

生成物 1

HCID 22568908(4-Bromo-3-isopropyl-phenoxy)-tert-butyl-dimethyl-silane収率 87%

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 6228
Dimethylformamide
溶媒

実験手順

A solution of 4-bromo-3-isopropyl-phenol (Intermediate 144, 1.13 g, 5.25 mmols), chloro-tert-butyl-dimethylsilane (0.95 g, 6.30 mmols), and imidazole (428.0 mg, 6.3 mmols) in 10 mL DMF was stirred at 25° C. for 3 hours. The solution was diluted with H2O and extracted with Et2O and the combined organic layers were washed with H2O, saturated aqueous NaCl, and dried (MgSO4) before being concentrated under reduced pressure. Column chromatography (1-2% EtOAc-hexanes) afforded 1.50 g (87%) of the title compound as a colorless oil.

後処理

  1. extractionextracted with Et2O
  2. washthe combined organic layers were washed with H2O, saturated aqueous NaCl
  3. dry with materialdried (MgSO4)
  4. concentrationbefore being concentrated under reduced pressure

出典と根拠

ORDレコード
ord-5021d5b60175447794991c8c4b8b8f2c
出典データセット
uspto-grants-2002_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06359135B1

反応ノート

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