HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 2-(4-Iodobutyl)-1H-isoindole-1,3(2H)-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | N-(4-Bromobutyl)phthalimide | HCID 93575 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-(4-Iodobutyl)-1H-isoindole-1,3(2H)-dione | HCID 230285 | 68.6% |
Reaction Steps
A solution of 5.0 g (0.018 mol) of N-(4-bromobutyl)phthalimide in 116 mL of acetone was treated with 20.7 g (0.125 mol) of potassium iodide and stirred at room temperature for 5 days. The reaction was filtered and the filtrate was diluted with 400 mL of ether, then filtered again through celite. The filtrate was concentrated at reduced pressure. The resulting solid was recrystallized from 300 mL of hexane (filtered hot and boiled down to 150 mL) to yield 4.0 g (68.6%) of 3 as white needles.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06063908 |
| Source dataset | uspto-grants-2000_05 |
| ORD ID | ord-bf79eda00a9c4761836bb5b1e604f93e |
| Source note | uspto-grants-2000_05 |