HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Fluoro-4-trimethylsilylnitrobenzene → 2-Fluoro-4-(trimethylsilyl)aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Fluoro-4-trimethylsilylnitrobenzene | HCID 59140187 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Fluoro-4-(trimethylsilyl)aniline | HCID 59596599 | 92% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07855216B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-b7a3bcbda79c45e7ae8d8719a1c94785 |
| Source note | uspto-grants-2010_12 |