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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073211Generated: November 2, 2026

Iodoethane → Ethyl 2-methylbenzo[d]imidazo[2,1-b]thiazole-3-carboxylate

https://huagongshe.com/reaction/1073211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantSodium hydrideHCID 24758—
ReactantHCID 13118865HCID 13118865—
SolventDimethylformamideHCID 6228—
ProductEthyl 2-methylbenzo[d]imidazo[2,1-b]thiazole-3-carboxylateHCID 1311885959.5%

Reaction Conditions

Temperature40 °C

Reaction Steps

Subsequently, 6.0 g of 2-methylimidazo[2,1-b]benzothiazole-3-carboxylic acid was suspended in 100 ml of dry dimethylformamide. Under ice cooling, 1.5 g of 60% sodium hydride was added to the suspension. After stirring for 30 minutes, 6.0 g of ethyl iodide was added to the mixture followed by heating at 40° C. overnight. After completion of the reaction, the solvent was removed under reduced pressure. Ether and water were added to the residue, which was fractionated. The residue obtained from the ether phase was crystallized with n-hexane to give 4.0 g of ethyl 2-methylimidazo[2,1-b]benzothiazole-3-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04968708
Source datasetuspto-grants-1990_11
ORD IDord-4f5eed6b59a64e7c8e4e621b3e391e2d
Source noteuspto-grants-1990_11