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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228051Generated: October 31, 2026

Imidazole → tert-Butyldimethyl((4-nitrobenzyl)oxy)silane

https://huagongshe.com/reaction/2228051

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantDimethylformamideHCID 6228—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant4-Nitrobenzyl alcoholHCID 69275—
SolventWaterHCID 962—
Producttert-Butyldimethyl((4-nitrobenzyl)oxy)silaneHCID 11065418100.2%

Reaction Steps

A mixture of 4-nitrobenzylalcohol(10.0 g), tert-butyl-dimethylsilyl chloride (11.8 g), imidazole (11.2 g) and DMF (50 ml) was stirred at room temperature for 1.5 hours. To the mixture was added water (500 ml), and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated sodium chloride solution, dried with anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was separated and purified with column chromatography (ethyl acetate/hexane=1/7) to give tert-butyldimethyl-4-nitrobenzyloxysilane (17.5 g) as pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06413947B1
Source datasetuspto-grants-2002_07
ORD IDord-913e31d130f540b1a34f37f778326fb4
Source noteuspto-grants-2002_07