HuagongsheHuagongshe Chemistry Print Report · For research reference only
9,10-Phenanthrenedione → 2-(3-Bromophenyl)dibenzo[f,h]quinoxaline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 9,10-Phenanthrenedione | HCID 6763 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1-(3-Bromophenyl)ethane-1,2-diamine | HCID 22756665 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(3-Bromophenyl)dibenzo[f,h]quinoxaline | HCID 86703824 | — |
Reaction Steps
First, into a 500-mL three-neck flask were put 2.5 g of 1-(3-bromophenyl)ethane-1,2-diamine, 0.62 g of potassium hydroxide, and 200 mL of dry ethanol, and the atmosphere in the flask was replaced with nitrogen. A reaction container was heated, the reacted solution was refluxed for two hours, 2.1 g of 9,10-phenanthrenequinone was added thereto, and the mixture was refluxed for nine hours. Then, the obtained mixture was subjected to suction filtration, and washed with ethanol, thereby obtaining 2-(3-bromophenyl)dibenzo[f,h]quinoxaline (a yellow white solid, a collection rate of 70%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09196844B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-fb463001fe3d4ce48b21cc095b6a1da3 |
| Source note | uspto-grants-2015_11 |