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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1277033Generated: October 26, 2026

tert-Butyldimethyl((4-nitrobenzyl)oxy)silane → 4-Aminobenzyloxy-tert-butyldimethylsilane

https://huagongshe.com/reaction/1277033

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyldimethyl((4-nitrobenzyl)oxy)silaneHCID 11065418—
SolventEthanolHCID 702—
Product4-Aminobenzyloxy-tert-butyldimethylsilaneHCID 1107547094.2%

Reaction Steps

In ethanol (80 ml) was dissolved tert-butyldimethyl-4-nitrobenzyloxysilane (16.5 g), and to the mixture was added dried 5% palladium on carbon (0.83 g). Under hydrogen atmosphere, the mixture was stirred at room temperature under atmospheric pressure for 7.5hours. The palladium was filtered off, and the filtrate was concentrated. The residue was separated and purified with column chromatography (ethyl acetate/hexane=1/4) to give 4-aminobenzyloxy-tert-butyldimethylsilane (13.8 g) as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06166006
Source datasetuspto-grants-2000_12
ORD IDord-d2b93e05d82747b2a58f3fc821d6adb4
Source noteuspto-grants-2000_12