HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanethiol → 6-Chloro-2-ethylsulfanyl-4-methyl-pyridine-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanethiol | HCID 6343 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2,6-Dichloro-4-methylpyridine-3-carboxylic acid | HCID 676121 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-Chloro-2-ethylsulfanyl-4-methyl-pyridine-3-carboxylic acid | HCID 86664312 | 95% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
6.1 g (153 mmol, 60% w/w in mineral oil) NaH were dissolved in THF (90 ml) at 0° C. At this temperature 3.4 g (54.7 mmol) ethane thiol were added. After stirring for 15 min at 0° C., 12.4 g (60.2 mmol) 2,6-dichloro-4-methyl-pyridine-3-carboxylic acid were added portionwise. The RM was allowed to warm to RT and stirring was continued at RT for 16 h. Then the reaction was quenched with a 2M aq. HCl and diluted with EtOAc. The organic layer was separated, dried over MgSO4 and concentrated in vacuo. Crystallisation (DCM/hexane) of the residue yielded 12.0 g (51.7 mmol, 95%) 6-chloro-2-ethylsulfanyl-4-methyl-pyridine-3-carboxylic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09278103B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-0a21c894d81c41a19c4eb8895f8969d1 |
| Source note | uspto-grants-2016_03 |