HuagongsheHuagongshe Chemistry Print Report · For research reference only
8-Hydroxyquinoline → p-Toluenesulfonic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 8-Hydroxyquinoline | HCID 1923 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 2-Methylbenzenesulfonic acid hydrate | HCID 12496995 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | p-Toluenesulfonic acid | HCID 6101 | — |
| Product | quinolin-1-ium-8-ol | HCID 5257170 | — |
Reaction Steps
The toluenesulfonic acid salt of 8-hydroxyquinoline was formed by dissolving toluenesulfonic acid monohydrate (1.9 g, 10 mmol) in acetonitrile and adding 8-hydroxyquinoline (1.45 g, 10 mmol). Removal of solvent in vacuo and addition of ether to the residual oil results in crystallization. Trituration several times with ether followed by drying in vacuo yields 8-hydroxyquinolinium, p-toluenesulfonate as a powder (3.11 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04587051 |
| Source dataset | uspto-grants-1986_05 |
| ORD ID | ord-3747068ec8514b65931ee3b110729e3e |
| Source note | uspto-grants-1986_05 |