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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095738Generated: October 25, 2026

Chloroacetaldehyde → 7-Ethylimidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1095738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetaldehydeHCID 33—
Reactant4-Ethylpyridin-2-amineHCID 118425—
SolventEthanolHCID 702—
Product7-Ethylimidazo[1,2-a]pyridineHCID 1818446398.6%

Reaction Steps

A mixture of 4-ethylpyridin-2-amine (3.21 g, 8.19 mmol), and chloroacetaldehyde (50% aqueous solution, 2.6 ml, 10.5 mmol) in EtOH (10 ml) was refluxed vigorously for 12 hours. The reaction mixture was concentrated, and the residue was suspended in saturated aqueous sodium bicarbonate solution. The aqueous mixture was extracted with CH2Cl2 and EtOAc, and the combined organic extracts were dried over Na2SO4, filtered and concentrated to afford the desired product (1.18 g, 98% yield) as a viscous oil. MS APCI (+) m/z 147.2 (M+1) detected.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138181B2
Source datasetuspto-grants-2012_03
ORD IDord-a14ef65495744592aceb2fbe75dcfb13
Source noteuspto-grants-2012_03