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
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-ethoxalyl-N-(2-phthalimido)ethyl-4-(2,2,3,3-tetrafluoropropoxy)aniline | HCID 86749721 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-[4-(2,2,3,3-Tetrafluoropropoxy)phenyl]-2,3-piperazinedione | HCID 19065084 | 36.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05545652 |
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| Source dataset | uspto-grants-1996_08 |
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| ORD ID | ord-19f1d9efca2245f6b9aff00eb92f300e |
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| Source note | uspto-grants-1996_08 |
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