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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576051Generated: November 2, 2026

4-(Trifluoromethyl)aniline → HCID 86707269, compound

https://huagongshe.com/reaction/576051

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)anilineHCID 9964—
ReactantHCID 59432940HCID 59432940—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
ProductHCID 86707269HCID 8670726970.7%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 4-trifluoromethyl aniline (213 μL, 1.70 mmol) in pyridine (270 μL) was added 2-(trichloroacetyl)-2,3-dihydro-1 H-isoindole-5-sulfonyl chloride (617 mg, 1.70 mmol) at room temperature, and the mixture was stirred at 60° C. for 1.5 hr. The reaction mixture was allowed to cool to room temperature and diluted with ethyl acetate. The mixture was washed with 1 mol/L hydrochloric acid, brine and water. The organic layer was dried over anhydrous sodium sulfate and then the desiccant was filtered off, followed by concentration under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=4:1→2:1) to afford the title compound as a colorless powder (586 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09035059B2
Source datasetuspto-grants-2015_05
ORD IDord-9c8a67ed87b74650aeb003c8cf2d7f1a
Source noteuspto-grants-2015_05