HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 5-(2-Fluoro-6-iodophenyl)-2-methyl-2H-tetrazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178505770 | HCID 178505770 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-(2-Fluoro-6-iodophenyl)-2-methyl-2H-tetrazole | HCID 16102901 | — |
Reaction Steps
A mixture of 5-(2-fluoro-6-iodophenyl)-1H-tetrazole (23.48 g, 80.97 mmol), potassium carbonate (16.79 g, 0.121 mol), and iodomethane (16.09 g, 0.113 mol) in 25 mL DMF was stirred at room temperature for 3 hours. The mixture was partitioned between ethyl acetate and water, and the organic extract was washed with water and brine, dried over Na2SO4, filtered and concentrated under vacuum. The residue was subjected to silica gel chromatography eluted with 0-10% ethyl acetate in hexanes to provide 5-(2-fluoro-6-iodophenyl)-2-methyl-2H-tetrazole that gave proton NMR spectra consistent with theory and a mass ion (ES+) of 305.06 for M+H+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06919343B2 |
| Source dataset | uspto-grants-2005_07 |
| ORD ID | ord-d655f2eb871848239b7d61ba4d41b849 |
| Source note | uspto-grants-2005_07 |