HuagongsheHuagongshe Chemistry Print Report · For research reference only
Furfural → 2-[2-(2-Furyl)ethenyl]-8-quinolinol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Furfural | HCID 7362 | — |
| Reactant | 2-Methyl-8-hydroxyquinoline | HCID 13224 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-[2-(2-Furyl)ethenyl]-8-quinolinol | HCID 54571506 | — |
Reaction Steps
A mixture of 8-hydroxyquinaldine (5.09 g) and 2-furaldehyde (8.0 mL) are heated at reflux overnight. The reaction is cooled to room temperature. The residue is taken up in acetone and adsorbed onto silica. A silica gel column eluting with 100% CH2Cl2 is run and the product-containing fractions evaporated under reduced pressure to give an orange/yellow oil. The product is crystallized with EtOH/H2O, filtered, washed thoroughly with water, and dried (1.18 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06310211B1 |
| Source dataset | uspto-grants-2001_10 |
| ORD ID | ord-578747debd2643f3b5fb58a36d4422c3 |
| Source note | uspto-grants-2001_10 |