HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856134Generated: October 29, 2026
Sodium Iodide → 5-(2-methyloxiran-2-ylmethylthio)-1-phenyl-1H-tetrazole
https://huagongshe.com/reaction/856134
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Methyloxiran-2-ylmethyl paratoluenesulfonate | HCID 14237194 | — |
| Reactant | 1-phenyltetrazole-5-thiol | HCID 178527986 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-(2-methyloxiran-2-ylmethylthio)-1-phenyl-1H-tetrazole | HCID 23081534 | 39% |
Reaction Steps
A mixture of 1-phenyl-5-mercapto-1H-tetrazole (3.5 g, 19.64 mmol), (2-methyl-2-oxiranylmethyl) toluene-4-sulfonate (5 g, 20.64 mmol), potassium carbonate (3 g, 21.71 mmol), and sodium iodide (4.5 g, 30.02 mmol) in DMF (30 ml) was stirred at 60° C. for 6 hours. The reaction mixture was was poured into water, and extracted with ethyl acetate twice. The extracts were combined, washed with 5% sodium hydroxide aqueous solution and then with water three times, and dried over sodium sulfate. After filtration, the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane/ethyl acetate=2/1) to afford 5-(2-methyl-2-oxiranylmethylsulfanyl)-1-phenyl-1H-tetrazole (1.9 g, yield 39%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07262212B2 |
|---|
| Source dataset | uspto-grants-2007_08 |
|---|
| ORD ID | ord-2a3832d3910c437199b83a667faa9980 |
|---|
| Source note | uspto-grants-2007_08 |
|---|