HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → ethyl 2-(5-methyl-1H-tetrazol-1-yl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2-(5-methyl-1H-tetrazol-1-yl)benzoic acid | HCID 12524192 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | ethyl 2-(5-methyl-1H-tetrazol-1-yl)benzoate | HCID 3761737 | 90.7% |
Reaction Steps
Under a nitrogen atmosphere, 2-(5-methyl-1H-tetrazol-1-yl)benzoic acid (89.7 g, 0.44 mol) was dissolved in acetone (1 L) and cesium carbonate (214.7 g, 0.66 mol) was added with vigorous stirring. Ethyl iodide (70.3 ml, 0.88 mol) was added dropwise and the reaction was heated to reflux for 4 hours. The reaction was cooled to room temperature and filtered. The acetone was removed in vacuo to yield a yellow solid which was dissolved in dichloromethane (800 ml) and washed with saturated sodium bicarbonate (200 ml). The organic fraction was dried (Na2SO4), filtered, and concentrated to yield 92.7 g of ethyl 2-(5-methyl-1H-tetrazol-1-yl)benzoate as a light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06664260B2 |
| Source dataset | uspto-grants-2003_12 |
| ORD ID | ord-e4eb31f9bf1543d98651871e1774795c |
| Source note | uspto-grants-2003_12 |