HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 8-(4-n-Butoxyphenylthio)-5,6,7,8-tetrahydroquinoline hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 8-(4-Hydroxyphenylthio)-5,6,7,8-tetrahydroquinoline | HCID 14281259 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 8-(4-n-Butoxyphenylthio)-5,6,7,8-tetrahydroquinoline hydrochloride | HCID 14281274 | — |
Reaction Steps
0.72 g (24 mmol) of sodium hydride were added to a solution of 5.15 g (20 mmol) of 8-(4-hydroxyphenylthio)-5,6,7,8-tetrahydroquinoline in 26 ml of dimethylformamide under nitrogen. When effervescence had ceased, 3.29 g (24 mmol) of n-bromobutane were added dropwise with ice-cooling. After stirring at room temperature overnight, the mixture was poured into ice-cold water and extracted with ether to obtain a brown oil. A solution of the oil in ether was treated with ethereal hydrogen chloride to precipitate 4.89 g (70%) of 8-(4-n-butoxyphhenylthio)-5,6,7,8-tetrahydroquinoline hydrochloride as pale yellow crystals (from ethanol-ether).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04847268 |
| Source dataset | uspto-grants-1989_07 |
| ORD ID | ord-d54716f5f8d34fa9952b2a73a841fcb1 |
| Source note | uspto-grants-1989_07 |