HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 1-Methyl-5-nitroquinolin-1-ium iodide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | 5-Nitroquinoline | HCID 11829 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Methyl-5-nitroquinolin-1-ium iodide | HCID 12495050 | — |
Reaction Steps
5-Nitroquinoline (4 g, 30 mmol) was melted at 85° C., prior to addition of dimethyl sulfate (2.2 ml, 30 mmol), and the resulting mixture was stirred at this temperature for 1.5 hours. The yellow gel was dissolved in water (35 ml) and cooled to room temperature. A saturated aqueous solution of potassium iodide (7.63 g, 45.9 mmol) was added, and the resulting orange precipitate was filtered, washing the residue with chilled water. After drying under vacuum at 60° C., for 2 hours, the brick-red solid was used in the next step without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07442701B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-ec8fbf85c3ab4e498eea5f7341e343fd |
| Source note | uspto-grants-2008_10 |