HuagongsheHuagongshe Chemistry Print Report · For research reference only
O-Phenylenediamine → Dipyridophenazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | O-Phenylenediamine | HCID 7243 | — |
| Reactant | 1,10-Phenanthroline-5,6-dione | HCID 72810 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Dipyridophenazine | HCID 3081616 | 55.1% |
Reaction Steps
Into a 200 mL recovery flask were placed 1,10-phenanthroline-5,6-dione (1.09 g, 5.19 mmol) and ethanol (10 mL), and the mixture was stirred to provide a suspension. And then, 1,2-phenylenediamine (0.592 g, 5.20 mmol) and ethanol (40 mL) were added to the suspension, and the mixture was refluxed for 2 hours. After allowing the reaction liquid to stand overnight, an insoluble substance was collected by filtration, and washed with cold ethanol. And then, the product was recrystallized with ethanol, and dipyrido[3,2-a:2′,3′-c]phenazine (Qxphen) (0.808 g) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08859894B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-f5321428c8204688b162573a415d0ebb |
| Source note | uspto-grants-2014_10 |