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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 497736Generated: October 27, 2026

Iodoethane → ethyl 2-(5-methyl-1H-tetrazol-1-yl)nicotinate

https://huagongshe.com/reaction/497736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(5-Methyl-1H-tetrazol-1-yl)nicotinic acidHCID 12132860—
SolventAcetoneHCID 180—
Productethyl 2-(5-methyl-1H-tetrazol-1-yl)nicotinateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06949646B2
Source datasetuspto-grants-2005_09
ORD IDord-5038a93e9222439a80572343fe9557f1
Source noteuspto-grants-2005_09