HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → ethyl 2-(5-methyl-1H-tetrazol-1-yl)nicotinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(5-Methyl-1H-tetrazol-1-yl)nicotinic acid | HCID 12132860 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | ethyl 2-(5-methyl-1H-tetrazol-1-yl)nicotinate | HCID 12132861 | — |
Reaction Steps
2-(5-Methyl-1H-tetrazol-1-yl)nicotinic acid (5.6 g, 27 mmole) was suspended in acetone (250 mL), potassium carbonate (5 g) and ethyl iodide (5 mL) were added and the reaction mixture was heated at reflux for 2 hours. The acetone was removed under vacuum. The residue was partitioned between water and dichloromethane. The dichloromethane layer was separated, dried, then concentrated under vacuum to provide 6.3 g of ethyl 2-(5-methyl-1H-tetrazol-1-yl)nicotinate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06747040B2 |
| Source dataset | uspto-grants-2004_06 |
| ORD ID | ord-2769254496f4452b901d35d07223eefe |
| Source note | uspto-grants-2004_06 |