HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → 7-Nitroisoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | 1,2,3,4-Tetrahydro-7-nitroisoquinoline | HCID 6424833 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 7-Nitroisoquinoline | HCID 12216277 | 37% |
Reaction Steps
Under refluxing, a solution of iodine (4.0 g, 15.9 mmol) in ethanol (56 mL) was added dropwise to a stirred solution of 31-2 (2.0 g, 9.34 mmol) in ethanol (24 mL) during 5 h. Then the resulted mixture was stirred for a further 66 h. The solvent was removed and the residual was loaded onto a silica gel chromatography column (PE:EA=6:1) to give 31-3 as a brown dark solid (602 mg, yield 36%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09138427B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-306dc68c78e24a3888084b710b03034c |
| Source note | uspto-grants-2015_09 |