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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1184197Generated: November 3, 2026

Phenol → Ethyl 3-(phenoxymethyl)imidazo[1,2-a]pyridine-2-carboxylate

https://huagongshe.com/reaction/1184197

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantTriethylamineHCID 8471—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 3-(chloromethyl)imidazo[1,2-a]pyridine-2-carboxylate hydrochlorideHCID 67320957—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductEthyl 3-(phenoxymethyl)imidazo[1,2-a]pyridine-2-carboxylateHCID 5835529539.8%

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of a mixture of phenol (2.20 g) and sodium hydride (95 wt %, 500 mg) in DMF (40 ml) was added dropwise to a solution of ethyl 3-(chloromethyl)imidazo[1,2-a]pyridine-2-carboxylate hydrochloride (3.5 g) in DMF (50 ml) at 0° C. Triethylamine (2.7 ml) was added at the same temperature over 30 min. The reaction mixture was stirred at 50° C. for 3 hr, and the reaction mixture was diluted with water and extracted with ethyl acetate. The extract was washed with saturated brine, 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 ethyl acetate-hexane (6:1) was concentrated under reduced pressure to give the object product (1.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08664380B2
Source datasetuspto-grants-2014_03
ORD IDord-98db07bc3aa84b21bea670019ab23423
Source noteuspto-grants-2014_03