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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844164Generated: October 27, 2026

Ethyl 8-(benzyloxy)-2,6-dimethylimidazo[1,2-a]pyridine-3-carboxylate → Ethyl 8-hydroxy-2,6-dimethylimidazo[1,2-a]pyridine-3-carboxylate

https://huagongshe.com/reaction/1844164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 8-(benzyloxy)-2,6-dimethylimidazo[1,2-a]pyridine-3-carboxylateHCID 86717926—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
ProductEthyl 8-hydroxy-2,6-dimethylimidazo[1,2-a]pyridine-3-carboxylateHCID 86717883—

Reaction Steps

74 g (228 mmol) of ethyl 8-(benzyloxy)-2,6-dimethylimidazo[1,2-a]pyridine-3-carboxylate Example 86A were initially charged in 1254 ml of dichloromethane and 251 ml of ethanol, and 20.1 g of 10% palladium on activated carbon (moistened with water 50%) were added under argon. The reaction mixture was hydrogenated overnight at RT and atmospheric pressure. The reaction mixture was filtered off through kieselguhr and concentrated. The crude product was purified by silica gel chromatography (dichloromethane:methanol=95:5). This gave 50.4 g (94% of theory) of the target compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946215B2
Source datasetuspto-grants-2015_02
ORD IDord-0685bd7ad0164a74b45deeeb386ad086
Source noteuspto-grants-2015_02