HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 2,5-Bis[(trifluoromethyl)sulfanyl]-1H-pyrrole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Pyrrole | HCID 8027 | — |
| Reactant | Methanesulfenyl chloride, trifluoro- | HCID 67900 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Carbon Dioxide | HCID 280 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2,5-Bis[(trifluoromethyl)sulfanyl]-1H-pyrrole | HCID 12508316 | — |
| Product | 2,4-Bis[(trifluoromethyl)sulfanyl]-1H-pyrrole | HCID 12508322 | — |
Reaction Steps
25 g of trifluoromethanesulfenyl chloride was condensed in a pressured bottle in dry ice and 2.34 g of pyrrole in 40 ml of anhydrous chloroform, 12.1 g of pyridine and 0.8 g of iron powder were added. The mixture was then stirred at room temperature for 3 days. It was then filtered to remove insoluble materials. The mixture was washed with water, diluted hydrochloric acid and water again. After evaporation of the solvent, the residue was distilled under vacuum, giving 4.2 g of 2,5-bis(trifluoromethylthio)pyrrole and 3.5 g 2,4-bis(trifluoromethylthio)pyrrole. The total yield was 82%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05538812 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-97155b9936e34cadbc7e11a8c90454f4 |
| Source note | uspto-grants-1996_07 |