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

HRID 24243
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인쇄 미리보기

반응식

HRID 24243 반응식
[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]
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참가 물질

6

반응물 3

HCID 795ImidazoleHCID 28928tert-Butyldimethylsilyl chlorideHCID 225688014-Bromo-3-isopropylphenol2회

생성물 1

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

시약·촉매·용매 2

HCID 962Water용매HCID 6228
Dimethylformamide
용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-2a3ed3e31a7c4f5e8d994625097a73e4
출처 데이터셋
uspto-grants-2005_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06855512B2

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