HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-(4-Chlorobutylthio)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Bromo-4-chlorobutane | HCID 81364 | — |
| Reactant | HCID 178418616 | HCID 178418616 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(4-Chlorobutylthio)pyridine | HCID 19079186 | 65.5% |
Reaction Steps
To a solution of 25.0 g (225 mmol) of 2-mercaptopyridine and 34.5 ml (247 mmol) of triethylamine in 300 ml of ethanol, 28.5 ml (247 mmol) of 1-bromo-4-chlorobutane was added with stirring under ice-cooling, and the mixture was stirred at room temperature for 16 hours. The solvent was distilled off and the residue was dissolved in chloroform. The solution was washed with saturated aqueous sodium bicarbonate and water, and dried. The solvent was distilled off and the residue was purified by column chromatography (eluent:ethyl acetate/hexane=1:3) to give 29.73 g of the desired compound (65.5% yield, pale yellow oil).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05561147 |
| Source dataset | uspto-grants-1996_10 |
| ORD ID | ord-7ddc31d15fb34448b12245705a36cfb7 |
| Source note | uspto-grants-1996_10 |