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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 410455Generated: October 25, 2026

Imidazole → ((3-Bromo-5-nitrobenzyl)oxy)(tert-butyl)dimethylsilane

https://huagongshe.com/reaction/410455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant(3-Bromo-5-nitrophenyl)methanolHCID 14866972—
SolventDimethylformamideHCID 6228—
Product((3-Bromo-5-nitrobenzyl)oxy)(tert-butyl)dimethylsilaneHCID 6743176893.5%

Reaction Steps

A solution of 3-bromo-5-nitrobenzyl alcohol (5 g, 21.5 mmol), in N,N-dimethylformamide (5 mL) was treated with tert-butyldimethylsilyl chloride (4.9 g, 32.3 mmol) and imidazole (2.5 g, 36.6 mmol) and stirred at room temperature for 14 h. The reaction was quenched with water and extracted with ethyl acetate (2×). The organic layer was dried over sodium sulfate, filtered, and concentrated. Purification by flash chromatography on silica (0-75% ethyl acetate in hexanes) afforded [(3-bromo-5-nitrobenzyl)oxy](tert-butyl)dimethylsilane (7.32 g, 20.1 mmol, 93% yield) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759366B2
Source datasetuspto-grants-2014_06
ORD IDord-02d77ed9143d4fda8cea5d789f2aa38f
Source noteuspto-grants-2014_06