Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888463Generated: November 1, 2026

Imidazole → 1-Bromo-4-[1-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-1-methylethyl]benzene

https://huagongshe.com/reaction/1888463

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant2-(4-Bromophenyl)propan-2-olHCID 12681920—
SolventDimethylformamideHCID 6228—
Product1-Bromo-4-[1-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-1-methylethyl]benzeneHCID 5826672546%

Reaction Steps

tert-Butyldimethylsilyl chloride (2.10 g, 14 mmol) was added to a mixture of 2-(4-bromophenyl)-propan-2-ol (2.0 g, 9.3 mmol) and imidazole (0.95 g 14 mmol) in DMF (30 mL) and the resultant mixture was stirred at 80° C. for 24 h. The mixture was concentrated to one third of the original volume then diluted with water (50 mL) and extracted with diethyl ether (3×50 mL). The combined organic layer was dried over anhydrous sodium sulfate, filtered and evaporated in vacuo. The resultant residue was purified by chromatography (silica, 50 g column, Si-SPE, 0-5% diethyl ether in pentane) to afford the title compound as a colourless oil (1.39 g, 46%). 1H NMR (MeOD, 400 MHz): 7.46-7.37 (m, 4H); 1.56 (s, 6H); 0.95-0.91 (m, 9H); 0.06 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501765B2
Source datasetuspto-grants-2013_08
ORD IDord-2c7baa7ea61e4e0a8533c4198525119f
Source noteuspto-grants-2013_08