HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73441Generated: October 28, 2026
1,2,3-Trifluoro-4-nitrobenzene → HCID 59386302, compound
https://huagongshe.com/reaction/73441
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2,3-Trifluoro-4-nitrobenzene | HCID 69871 | — |
| Reactant | 2-Fluoro-4-iodoaniline | HCID 185694 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59386302 | HCID 59386302 | — |
Reaction Steps
To a solution of 2-fluoro-4-iodoaniline (11.40 g, 47 mmol) in 100 ml anhydrous THF at 0° C., 47 ml of a 1M solution of LHMDS in THF (47 mmol) was added dropwise. The color of the solution turned dark purple. The solution was transferred via cannula to a dropping funnel, and the solution (containing the amine free base) was added in small portions to a solution of 2,3,4-trifluoronitrobenzene (8.321 g, 47.0 mmol) in anhydrous THF (50 ml) at 0° C. After completion of addition the mixture was stirred under argon at room temperature for 15 hours. The volume of the solvent was reduced, followed by extraction using ethyl acetate and brine. The organic layer was dried over sodium sulfate, the solvent was removed, and the obtained dark oil was purified by flash chromatography (EtOAc/hexane 1:5, Rf=0.58) yielding the crude product, which became a brown solid upon drying in vacuo (yield: 6.23 g, 33.6%). m/z=393 [M−1]−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08829052B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-85289127abcf458eb315634e8a60bbca |
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| Source note | uspto-grants-2014_09 |
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