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

HRID 381147
Notes
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Reaction equation

HRID 381147 reaction equation
[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]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 3

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

Product 1

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

Reagents, catalysts & solvents 2

HCID 962WaterSolvent
HCID 6228
Dimethylformamide
Solvent

Procedure

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.

Workup

  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

Sources & evidence

ORD record
ord-e62b20f08d6943cabb3f2472c7ea82c5
Source dataset
uspto-grants-2001_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06303785B1

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes