Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2405555Generated: November 2, 2026

1,2,3-Trifluoro-4-nitrobenzene → HCID 59386302, compound

https://huagongshe.com/reaction/2405555

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2,3-Trifluoro-4-nitrobenzeneHCID 69871—
Reactant2-Fluoro-4-iodoanilineHCID 185694—
ReactantLithium HexamethyldisilazideHCID 2733832—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59386302HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08808742B2
Source datasetuspto-grants-2014_08
ORD IDord-9b6b3b169c7147d9b37f13be452afec3
Source noteuspto-grants-2014_08