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, followed by heating under reflux for 7 hours. After the reaction mixture was allowed to cool down to room temperature, 200 ml of petroleum ether were added and the resulting precipitate was collected by filtration. Further, the mother liquor was concentrated under reduced pressure and the residue was recrystallized from diethyl ether, whereby 13.6 g of the title compound were obtained (yield: 35%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06046212 |
| Source dataset | uspto-grants-2000_04 |
| ORD ID | ord-bf1bed581af64984aba6621c42e7788e |
| Source note | uspto-grants-2000_04 |