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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264955Generated: November 1, 2026

2-Fluoro-4-trimethylsilylnitrobenzene → 2-Fluoro-4-(trimethylsilyl)aniline

https://huagongshe.com/reaction/2264955

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoro-4-trimethylsilylnitrobenzeneHCID 59140187—
SolventEthanolHCID 702—
Product2-Fluoro-4-(trimethylsilyl)anilineHCID 5959659992%

Reaction Steps

The 2-fluoro-4-trimethylsilylnitrobenzene (5.45 g, 25.6 mmol) was then dissolved in ethanol (100 mL), transferred to a Parr shaker bottle, flushed with nitrogen, then charged with 10% Pd—C (0.4 g). The reaction mixture was hydrogenated for 1 h on the Parr apparatus (45 psi H2), and then filtered through a plug of Celite. The filter cake was washed with ethanol, and the combined filtrates were concentrated. The resulting residue was purified by flash chromatography (250 mL silica gel, 95:5 hexane-ethyl ether), to afford the title compound as a tan oil (4.31 g, 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855216B2
Source datasetuspto-grants-2010_12
ORD IDord-b7a3bcbda79c45e7ae8d8719a1c94785
Source noteuspto-grants-2010_12