HuagongsheHuagongshe Chemistry Print Report · For research reference only
8-Hydroxyquinoline → HCID 178524122, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 8-Hydroxyquinoline | HCID 1923 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | HCID 86584703 | HCID 86584703 | — |
| Solvent | Glycol monoethyl ether | HCID 8076 | — |
| Product | HCID 178524122 | HCID 178524122 | 57% |
Reaction Steps
4.7 mmol (0.68 g) of 8-hydroxyquinoline was added to a room-temperature solution of 0.14 mmol 2-phenylbenzothiazole Iridium chloride dimer (0.19 g) in 20 mL of 2-ethoxyethanol. Approximately 700 mg of sodium carbonate was added, and the mixture was heated to reflux under nitrogen in an oil bath overnight (23 hrs.). Reaction mixture was cooled to room temperature, and the red precipitate was filtered off via vacuum. The filtrate was concentrated and methanol was added to precipitate more product. Successive filtrations and precipitations afforded a 57% yield. The emission spectrum is in FIG. 43 and the proton NMR spectrum is in FIG. 44.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07537844B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-f2e8860e6185437880139aafc2cd18d4 |
| Source note | uspto-grants-2009_05 |