HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 3-Phenylquinolin-2-thione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | 2-Chloro-3-phenylquinoline | HCID 4256078 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Phenylquinolin-2-thione | HCID 13200206 | — |
Reaction Steps
A mixture of 2-chloro-3-phenylquinoline (3.4 g.) and thiourea (1.2 g.) in ethanol (20 ml.) was refluxed for one hour. The solution was allowed to cool to ambient temperature and diethyl ether (10 ml.) was added. The solid which precipitated was filtered off, dispersed in M-sodium hydroxide (70 ml.), and heated on a steam bath for 2 hr. The reaction mixture was acidified with 2 M-hydrochloric acid. The resulting mixture was filtered, and the solid residue was stirred with hot ethanol (50 ml.) and filtered. There was thus obtained as the solid residue 3-phenylquinolin-2-thione, m.p. 242°-4°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04435405 |
| Source dataset | uspto-grants-1984_03 |
| ORD ID | ord-7477dd82260441f6b87c6158416abdc1 |
| Source note | uspto-grants-1984_03 |