HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Hydroxyquinoline → Quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Hydroxyquinoline | HCID 69141 | — |
| Solvent | Phosphorus oxychloride | HCID 24813 | — |
| Product | Quinoline | HCID 7047 | 79.4% |
Reaction Steps
3-butyryl-6-benzoyloxymethyl)-4(1H)-quinolone (30 g) was heated under reflux in phosphorus oxychloride (200 ml) for 30 minutes. The solvent was evaporated and the residue partitioned between dichloromethane and ammonia solution. The organic layer was washed successively with sodium hydrogen carbonate solution and 50% brine. Dried anhyd. MgSO4), filtered and evaporated to an oily solid which crystallized on trituration with petroleum ether to give 3-butyryl-4-chloro-6-benzyloxymethyl)quinoline (21.2 g, 67%), m.p. 85° C.-6° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05089504 |
| Source dataset | uspto-grants-1992_02 |
| ORD ID | ord-14c173a9bff4469eb6fc04397d1b6174 |
| Source note | uspto-grants-1992_02 |