HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methylquinoline → HCID 621053, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methylquinoline | HCID 7060 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Terephthalaldehyde | HCID 12173 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 621053 | HCID 621053 | 35% |
Reaction Steps
1,4-Benzenedialdehyde (30 g, 0.22 mol), 2-methylquinoline (21 g, 0.15 mol) and acetic anhydride (41.5 ml, 0.40 mol) were dissolved in 160 ml of xylene. The resulting mixture was refluxed for 7 hours. After the mixture was allowed to cool down to room temperature, it was added to 200 ml of petroleum ether which had been warmed to 40-60° C. The resulting precipitate was filtered off. The mother liquor was concentrated and the crude product so obtained was recrystallized twice from etnanol, whereby 13.6 g of the title compound were obtained (yield: 35%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06136848 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-c60b79efdcfd4146ad45f9f902fe89ca |
| Source note | uspto-grants-2000_10 |