HuagongsheHuagongshe Chemistry Print Report · For research reference only
Veratryl alcohol → 8-Hydroxy-4-(3,4-dimethoxybenzyloxy)-2-methylquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Veratryl alcohol | HCID 7118 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Chloro-8-hydroxy-2-methylquinoline | HCID 12219722 | — |
| Solvent | 1,3-Dimethyl-2-imidazolidinone | HCID 6661 | — |
| Product | 8-Hydroxy-4-(3,4-dimethoxybenzyloxy)-2-methylquinoline | HCID 22113286 | 62.8% |
Reaction Steps
To a stirred solution of 3,4-dimethoxybenzyl alcohol (1.68 g) in 1,3-dimethyl-2-imidazolidinone (10 ml) was added sodium hydride (60% in oil, 400 mg) portionwise in an ice-water bath under a nitrogen atmosphere. The mixture was stirred for 30 minutes and then 4-chloro-8-hydroxy-2-methylquinoline (770 mg) was added thereto. The reaction mixture was stirred at 150° C. for 3 hours and cooled to ambient temperature followed by partition into ethyl acetate and water. The organic layer was washed with water twice, dried over magnesium sulfate and evaporated in vacuo. The residue was washed with diethyl ether to give a pale yellow powder (812 mg) of 8-hydroxy-4-(3,4-dimethoxybenzyloxy)-2-methylquinoline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05563162 |
| Source dataset | uspto-grants-1996_10 |
| ORD ID | ord-e4401e4a8059428f98d3750ea6a202cd |
| Source note | uspto-grants-1996_10 |