HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → Ethyl 5-acetoxy-2-(5-methyltetrazol-1-yl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 5-Acetoxy-2-(5-methyltetrazol-1-yl)benzoic acid | HCID 67050990 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Ethyl 5-acetoxy-2-(5-methyltetrazol-1-yl)benzoate | HCID 67051123 | 92.2% |
Reaction Steps
Cesium carbonate (176 g, 1.13 mol) was added to a solution of 5-acetoxy-2-(5-methyltetrazol-1-yl)benzoic acid (164 g, 0.620 mol) in 1.8 L of acetone. The mixture was stirred vigorously and iodoethane (116 g, 0.682 mol) diluted with 100 mL of acetone was added dropwise over a one-hour period. The reaction was stirred overnight at ambient temperature and was then concentrated under reduced pressure. The resulting solid was partitioned between dichloromethane and water. The aqueous fraction was extracted with dichloromethane and the combined organic fractions were dried over sodium sulfate, filtered, and concentrated to give 166 g of ethyl 5-acetoxy-2-(5-methyltetrazol-1-yl)benzoate as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07897597B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-46d1a8f35cee4a87af63120b17e146fa |
| Source note | uspto-grants-2011_03 |