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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384219Generated: November 2, 2026

Imidazole → 1-(Tert-butyldimethylsiloxy)-2-methyl-3-(4-bromophenyl)propane

https://huagongshe.com/reaction/1384219

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant3-(4-Bromophenyl)-2-methylpropan-1-olHCID 21714199—
SolventDimethylformamideHCID 6228—
Product1-(Tert-butyldimethylsiloxy)-2-methyl-3-(4-bromophenyl)propaneHCID 2118636095.1%

Reaction Steps

A solution of imidazole (27.2 g) in DMF (100 ml) was added to a stirred solution of 2-methyl-3-(4-bromophenyl)propanol (37.4 g) and tert-butyldimethylsilyl chloride (28.9 g) in dry DMF (100 ml) at 0° C. The reaction mixture was allowed to stir, warming to ambient temperature, over 21 hours and was then poured onto ice (500 g). The reaction mixture was extracted with diethyl ether (3×500 ml), the combined organic layers were dried (MgSO4) and the solvent was evaporated to give 1-(tert-butyldimethylsiloxy)-2-methyl-3-(4-bromophenyl)propane as a yellow oil (53.3 g), mass spectrum (+ve CI): 343 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06258817B1
Source datasetuspto-grants-2001_07
ORD IDord-42462cd02f5f4ad7909f443306eeee98
Source noteuspto-grants-2001_07