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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 406276Generated: October 30, 2026

Acetic Acid → Ethyl 3-(hydroxymethyl)imidazo[1,2-a]pyridine-8-carboxylate

https://huagongshe.com/reaction/406276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantFormaldehydeHCID 712—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium AcetateHCID 517045—
ReactantEthyl imidazo[1,2-a]pyridine-8-carboxylateHCID 10867135—
SolventWaterHCID 962—
ProductEthyl 3-(hydroxymethyl)imidazo[1,2-a]pyridine-8-carboxylateHCID 5998456586.9%

Reaction Steps

A mixture of ethyl imidazo[1,2-a]pyridine-8-carboxylate (1 g, 5.26 mmol), sodium acetate (1.725 g, 21.03 mmol), formaldehyde (36.5% wt. in water, 2.5 mL, 33.1 mmol) and acetic acid (1.145 mL, 20 mmol) was stirred at room temperature for 3 hours. The reaction mixture was then heated at reflux for a further 4 hours and then cooled and diluted with water (50 mL). The pH was adjusted to 8 with saturated aqueous sodium hydrogen carbonate solution (ca. 10 mL) and the solution was extracted successively with ethyl acetate (3×50 mL) and 3:1 chloroform:isopropanol (100 mL). The organic extracts were combined, washed successively with saturated sodium bicarbonate (50 mL) and brine (50 mL) and dried (MgSO4), filtered and the solvent evaporated in vacuo. The residue was dissolved in dichloromethane and purified on a silica cartridge (100 g) using a 0-30% methanol (+1% Et3N)-DCM gradient over 60 mins. The product containing fractions were combined and evaporated in vacuo to give the title compound as a colourless oil (1.007 g)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754101B2
Source datasetuspto-grants-2014_06
ORD IDord-3897466a9a94443bb406a6c7767e7c94
Source noteuspto-grants-2014_06