HuagongsheHuagongshe Chemistry Print Report · For research reference only
O-Phenylenediamine → 2-Methyl-3-phenylquinoxaline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | O-Phenylenediamine | HCID 7243 | — |
| Reactant | 1-Phenyl-1,2-propanedione | HCID 11363 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-Methyl-3-phenylquinoxaline | HCID 346903 | 98% |
Reaction Steps
3.23 g of 1-phenyl-1,2-propanedione and 2.48 g of 1,2-phenylendiamine were refluxed in a chloroform solvent in nitrogen atmosphere for 4 hours. An organic layer was washed with 1 mol/L hydrochloric acid, and washed with a saturated salt solution, then, dried. The solvent was distilled off to give a ligand, 2-methyl-3-phenylquinoxaline (abbreviated as Hmpq) (pale orange powder, yields of 98%). A synthesis scheme of the step 1 (b-1) is represented as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07795429B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-47649842841e4df889cd0466f21c1295 |
| Source note | uspto-grants-2010_09 |