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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1277032Generated: October 26, 2026

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

https://huagongshe.com/reaction/1277032

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), tertbutyl-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 numberUS06166006
Source datasetuspto-grants-2000_12
ORD IDord-7c8f710559964c61a31220db588578ab
Source noteuspto-grants-2000_12