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 | 69.7% |
Reaction Steps
8.2 g (29 mmol) of 1-(4-bromophenyl)-2-phenylethanedione, 3.1 g (31 mmol) of o-phenylenediamine, and 100 mL of ethanol were placed into a 300-mL flask, and the mixture was refluxed for 2 hours. After the reaction, the precipitated solid was collected by suction filtration. The collected solid washed with ethanol and dried. 7.3 g of a light-yellow solid was obtained as the target substrate in 69% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07696348B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-351ebe2be7e44c089e1b72b9d6519b7a |
| Source note | uspto-grants-2010_04 |