Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482052Generated: October 30, 2026

Potassium Iodide → N-(2-phthalimido)ethyl-4-(2,2,3,3-tetrafluoropropoxy)aniline

https://huagongshe.com/reaction/482052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant1H-Isoindole-1,3(2H)-dione, 2-(2-bromoethyl)-HCID 11325—
ReactantPotassium BicarbonateHCID 516893—
Reactant4-(2,2,3,3-Tetrafluoropropoxy)anilineHCID 18766325—
SolventDimethylformamideHCID 6228—
ProductN-(2-phthalimido)ethyl-4-(2,2,3,3-tetrafluoropropoxy)anilineHCID 1906509841.1%

Reaction Steps

A mixture of 4-(2,2,3,3-tetrafluoropropoxy)aniline (7.4 g), N-(2-bromoethyl)phthalimide (9.0 g), potassium bicarbonate (6.9 g), potassium iodide (5.5 g) and N,N-dimethylformamide (80 ml) are refluxed for 22 hours. The solvent was distilled off under reduced pressure. To the residue, ice-water (200 ml) and ethyl acetate (200 ml) were added and fractionated. The ethyl acetate layer was washed with water, dried over anhydrous magnesium sulfate and distilled off under reduced pressure. The residue was purified by silica gel chromatography (eluate; ethyl acetate:hexane=1:2 v/v) and recrystallized from ethyl acetate-diisopropyl ether to give N-(2-phthalimido)ethyl-4-(2,2,3,3-tetrafluoropropoxy)aniline (5.4 g) as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05792780
Source datasetuspto-grants-1998_08
ORD IDord-5ef2bfb864914e8ea758dd7d32bb027b
Source noteuspto-grants-1998_08