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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1077902Generated: October 29, 2026

N-ethoxalyl-N-(2-phthalimido)ethyl-4-(2,2,3,3-tetrafluoropropoxy)aniline → 1-[4-(2,2,3,3-Tetrafluoropropoxy)phenyl]-2,3-piperazinedione

https://huagongshe.com/reaction/1077902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-ethoxalyl-N-(2-phthalimido)ethyl-4-(2,2,3,3-tetrafluoropropoxy)anilineHCID 86749721—
SolventEthanolHCID 702—
Product1-[4-(2,2,3,3-Tetrafluoropropoxy)phenyl]-2,3-piperazinedioneHCID 1906508436.5%

Reaction Steps

The mixture of the obtained N-ethoxalyl-N-(2-phthalimido)ethyl-4-(2,2,3,3-tetrafluoropropoxy)aniline (3.4 g), hydradine hydrate (0.7 ml) and ethanol (80 ml) was refluxed for 9 hours. The crystals separated out were filtered off before cooling and the solvent of the filtrate was distilled off under reduced pressure. Water (150 ml) and ethyl acetate (300 ml) were added to the residue to fractionate. The ethyl acetate layer was washed with 5% aqueous solution of sodium bicarbonate and then with a saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure. The residue was purified by silica gel chromatography (eluent; ethyl acetate:dichloromethane:methanol=7:7:1 v/v) to give 1-[4-(2,2,3,3-tetrafluoropropoxy)phenyl]-2,3-piperazinedione (0.8 g) as a colorless powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05545652
Source datasetuspto-grants-1996_08
ORD IDord-19f1d9efca2245f6b9aff00eb92f300e
Source noteuspto-grants-1996_08