HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroform → 3-[5-(Methanesulfonyl)-4-methyl-4H-1,2,4-triazol-3-yl]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Potassium Permanganate | HCID 516875 | — |
| Reactant | 3-(4-Methyl-5-(methylthio)-4H-1,2,4-triazol-3-yl)pyridine | HCID 40424626 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-[5-(Methanesulfonyl)-4-methyl-4H-1,2,4-triazol-3-yl]pyridine | HCID 46928334 | 53% |
Reaction Steps
KMnO4 (5 g, 32 mmol) was added to a solution of 3-[4-methyl-5-(methylthio)-4H-1,2,4-triazol-3-yl]pyridine (6.0 g, 29 mmol) in H2O (40 mL) and acetic acid (100 mL). After 1 h stirring at rt the reaction was basified with aq. NaOH (4M). CHCl3 was added and the mixture was filtrated through celite. The layers were separated and the water phase was washed with CHCl3. The combined organic phase was dried and concentrated to give 3.67 g (53%) of the title compound. 1H NMR: 3.59 (s, 3H) 3.99 (s, 3H) 7.52 (m, 1H) 8.02 (dt, 1H) 8.83 (dd, 1H) 8.91 (m, 1H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07585881B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-6294cd95bcec49d2a07551f1e036507c |
| Source note | uspto-grants-2009_09 |