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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 603336Generated: October 26, 2026

Hydrochloric Acid → N-(4-Ethylphenyl)-2,3,5,6-tetrafluoroaniline

https://huagongshe.com/reaction/603336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2,3,5,6-TetrafluoroanilineHCID 12786—
Reactant1-Bromo-4-ethylbenzeneHCID 15313—
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
ReactantSodium t-butoxideHCID 23676156—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductN-(4-Ethylphenyl)-2,3,5,6-tetrafluoroanilineHCID 21938675—

Reaction Conditions

Temperature85 °C

Reaction Steps

A mixture of 2,3,5,6-tetrafluoroaniline (4.5 g, 27.3 mmol), 4-ethylbromobenzene (5.0 g, 27 mmol), toluene (50 ml), sodium tert-butoxide (4.67 g, 48 mmol), tri-tert-butylphosphin (217 mg, 1.07 mmol) and bis-dibenzylideneacetone-palladium(0) (260 mg, 0.45 mmol) is heated under nitrogen to 85° C. for 15.5 h. The mixture is cooled to room temperature and water (30 ml), concentrated hydrochloric acid (20 ml) and hyflo are added. After stirring for 45 minutes, the mixture is filtered and the organic phase is washed with water three times. The solvent is evaporated in vacuo and the residue is chromatographed on silica using hexane/toluene (9:1 to 3:1) affording N-(2′,3′,5′,6′-tetrafluorophenyl)-4-ethylanilin as a liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906677B2
Source datasetuspto-grants-2011_03
ORD IDord-db7c28842a0549feb90e747c0c7962f1
Source noteuspto-grants-2011_03