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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1509530Generated: October 30, 2026

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

https://huagongshe.com/reaction/1509530

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 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 numberUS09221836B2
Source datasetuspto-grants-2015_12
ORD IDord-d6155a99f3994edebac34139c247fd91
Source noteuspto-grants-2015_12