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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419926Generated: October 25, 2026

tert-Butyldimethyl(4-nitrophenoxy)silane → 4-((Tert-butyldimethylsilyl)oxy)aniline

https://huagongshe.com/reaction/1419926

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyldimethyl(4-nitrophenoxy)silaneHCID 532659—
SolventMethanolHCID 887—
SolventPalladiumHCID 23938—
Product4-((Tert-butyldimethylsilyl)oxy)anilineHCID 11715553987.9%

Reaction Steps

tert-Butyl-dimethyl-(4-nitro-phenoxy)-silane (7.3 g, 2.9 mmol) was dissolved in MeOH (75 ml) and hydrogenated in the presence of Pd on C (10%, E 101 N/D) at room temperature and atmospheric pressure for 1 hour. The catalyst was filtered and the solvent was evaporated to provide 4-(tert-Butyl-dimethyl-silanyloxy)-phenylamine (6.4 g, 99%) as light yellow oil, MS: m/e=223 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05889026
Source datasetuspto-grants-1999_03
ORD IDord-4f9efee849d54062a00c4c5e8ae3141e
Source noteuspto-grants-1999_03