HuagongsheHuagongshe Chemistry Print Report · For research reference only
O-Phenylenediamine → 2-(4-Bromophenyl)-3-phenylquinoxaline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | O-Phenylenediamine | HCID 7243 | — |
| Reactant | 1-(4-Bromophenyl)-2-phenylethane-1,2-dione | HCID 236701 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(4-Bromophenyl)-3-phenylquinoxaline | HCID 1849790 | — |
Reaction Steps
In a 200 mL recovery flask were placed 4.5 g (15 mmol) of 1-(4-bromophenyl)-2-phenylethanedione, 1.8 g (17 mmol) of 1,2-phenylenediamine, and 50 mL of ethanol. This solution was refluxed under nitrogen stream for 2.5 hours. After a predetermined time, the solution was cooled to room temperature, and the precipitated solid was collected by suction filtration. The collected solid was washed with ethanol, so that 5.2 g of target white powder was obtained with a yield of 92%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08119259B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-26f53eccf1874b5db86c7fdef6f50ce4 |
| Source note | uspto-grants-2012_02 |