HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 5-(Methylsulfonyl)-2-(4-((trifluoromethyl)thio)phenoxy)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-(Trifluoromethylsulfanyl)phenol | HCID 3815158 | — |
| Reactant | 2,5-Bis(methylsulfonyl)pyridine | HCID 13102675 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(Methylsulfonyl)-2-(4-((trifluoromethyl)thio)phenoxy)pyridine | HCID 13102690 | 60% |
Reaction Steps
To 4.95 g of 4-(trifluoromethylthio)phenol dissolved in a 20 ml THF/20 ml DMSO mixture was added 2.9 g of t-BuOK and then 6.0 g of 2,5-bis(methylsulfonyl)pyridine, and the resulting mixture heated at 58° C. for 11/2 hrs. The reaction mixture was cooled to room temperature and added to approximately 3 to 4 volumes of water. The yellow-brown precipitate that formed was removed by filtration and then recrystallized from CH2Cl2 /ethanol. The purified product, 5-(methylsulfonyl)-2-(4-((trifluoromethyl)thio)phenoxy)pyridine, (60% yield), was recovered as tiny cream-white plates, m.p. 134°-135° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04616087 |
| Source dataset | uspto-grants-1986_10 |
| ORD ID | ord-cd1f68a202af4a62b731028261db1275 |
| Source note | uspto-grants-1986_10 |