Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505925Generated: November 1, 2026

Imidazole → 4-Bromobenzyloxy-tert-butyldimethylsilane

https://huagongshe.com/reaction/1505925

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant4-Bromobenzyl alcoholHCID 70119—
SolventDimethylformamideHCID 6228—
Product4-Bromobenzyloxy-tert-butyldimethylsilaneHCID 10859583100%

Reaction Steps

tert-Butyldimethylsilyl chloride (2.42 g, 16 mmol) was added to a mixture of (4-bromophenyl)methanol (2.0 g, 107 mmol) and imidazole (1.09 g, 16 mmol) in DMF (30 mL) and the resultant mixture was stirred at ambient temperature for 72 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 (3.21 g, 100%). NMR (CDCl3, 400 MHz): 7.45-7.42 (m, 2H); 7.21-7.17 (m, 2H); 4.68 (s, 2H); 0.93 (s, 9H); 0.09 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216980B2
Source datasetuspto-grants-2015_12
ORD IDord-fff8f7c567d14b22888460118dc87ba3
Source noteuspto-grants-2015_12