HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168562Generated: October 26, 2026
Iodoethane → ethyl 2-(5-methyl-1H-tetrazol-1-yl)benzoate
https://huagongshe.com/reaction/1168562
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(5-methyl-1H-tetrazol-1-yl)benzoic acid | HCID 12524192 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | ethyl 2-(5-methyl-1H-tetrazol-1-yl)benzoate | HCID 3761737 | 87.5% |
Reaction Steps
Acetone (3.2 L) and 2-(5-methyl-1H-tetrazol-1-yl)benzoic acid (228 g) were combined then stirred at ambient temperature for 15 minutes. Potassium carbonate (228 g) was added to the reaction mixture in a single portion. Iodoethane (366.8 g) was added dropwise to the reaction mixture producing a slight exotherm. The reaction mixture was heated at reflux for about 4 hours then stirred overnight while cooling to ambient temperature. The precipitated salts were removed by filtration then rinsed with acetone. The combined filtrates were evaporated under vacuum. The residue was dissolved in dichloromethane (1.5 L). The dichloromethane solution was washed with water (1.5 L), dried over magnesium sulfate then concentrated under vacuum to provide 227 g of ethyl-2-(5-methyl-1H-tetrazol-1-yl)benzoate as a white solid m.p. 98-100° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06624305B2 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-2c12814be6e74c5db974adbe5dc097d8 |
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| Source note | uspto-grants-2003_09 |
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