HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 4H-1,2,4-Triazole, 4-methyl-3-(methylthio)-5-(2-naphthalenyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 10243410 | HCID 10243410 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4H-1,2,4-Triazole, 4-methyl-3-(methylthio)-5-(2-naphthalenyl)- | HCID 3087999 | — |
Reaction Steps
A mixture of 2,4-dihydro-4-methyl-5-(2-naphthyl)-3-H-1,2,4-triazole-3-thione (5.26 g, 2.18×10-2 mole), K2CO3 (3.01 g, 2.18×10-2 mole), methyl iodide (1.5 ml, 2.4×10-2 mole), and acetone (65 ml) was stirred and warmed to reflux. After refluxing overnight, the solvent was evaporated at reduced pressure and the concentrate was treated with water. The aqueous mixture was extracted with EtOAc three times. The EtOAc extracts were combined, washed with saturated aqueous NaCl, and dried over anhydrous Na2SO4. The drying agent was removed by filtration and the filtrate was evaporated at reduced pressure to yield the desired product Mp 177°-179° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04981863 |
| Source dataset | uspto-grants-1991_01 |
| ORD ID | ord-bb8e489f5dea41e8ac215c2c44cd7519 |
| Source note | uspto-grants-1991_01 |