HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → 7-Iodo-4-(furan-2-yl)isoindolinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Tert-Butyl nitrite | HCID 10906 | — |
| Reactant | 7-Amino-4-(furan-2-yl)isoindolinone | HCID 68492739 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 7-Iodo-4-(furan-2-yl)isoindolinone | HCID 68487487 | 58% |
Reaction Steps
In a similar manner to Step 4 of Example 140, 7-amino-4-(furan-2-yl)isoindolinone (43.0 mg, 0.201 mmol) was dissolved in acetonitrile (4.3 mL), and the solution was treated with potassium iodide (40.0 mg, 0.241 mmol), copper iodide (46.0 mg, 0.241 mmol), iodine (61.0 mg, 0.241 mmol) and tert-butyl nitrite (0.072 mL, 0.60 mmol), followed by purification by preparative thin-layer chromatography (chloroform/acetonitrile=6/1) to obtain 7-iodo-4-(furan-2-yl)isoindolinone (37.8 mg, yield 58%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07745641B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-af72a1588c2f4fcfb3ce709ff335d054 |
| Source note | uspto-grants-2010_06 |