Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509528Generated: October 30, 2026

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

https://huagongshe.com/reaction/1509528

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium HydroxideHCID 14798—
ReactantSodium AcetateHCID 517045—
ReactantEthyl imidazo[1,2-a]pyridine-2-carboxylateHCID 818807—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
ProductEthyl 3-(hydroxymethyl)imidazo[1,2-a]pyridine-2-carboxylateHCID 1846690136.3%

Reaction Steps

To a solution of ethyl imidazo[1,2-a]pyridine-2-carboxylate (5.0 g) in acetic acid (30 ml) were added 37% formaldehyde (14 ml) and sodium acetate (8.0 g) at room temperature, and the reaction mixture was heated under reflux for 15 hr. The reaction mixture was cooled to room temperature and dissolved in dichloromethane. The mixture was adjusted to pH 8 with 10% aqueous sodium hydroxide solution at 0° C. The organic layer was separated, washed with water and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was subjected to silica gel column chromatography, and a fraction eluted with dichloromethane-methanol (15:1) was concentrated under reduced pressure to give the object product (2.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221836B2
Source datasetuspto-grants-2015_12
ORD IDord-3e8467486f3943a7b36a78b44d61d239
Source noteuspto-grants-2015_12