HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → N-(2-phthalimido)ethyl-4-(2,2,3,3-tetrafluoropropoxy)aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 1H-Isoindole-1,3(2H)-dione, 2-(2-bromoethyl)- | HCID 11325 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | 4-(2,2,3,3-Tetrafluoropropoxy)aniline | HCID 18766325 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(2-phthalimido)ethyl-4-(2,2,3,3-tetrafluoropropoxy)aniline | HCID 19065098 | 41.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05792780 |
| Source dataset | uspto-grants-1998_08 |
| ORD ID | ord-5ef2bfb864914e8ea758dd7d32bb027b |
| Source note | uspto-grants-1998_08 |