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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2169010Generated: November 1, 2026

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

https://huagongshe.com/reaction/2169010

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 numberUS09045436B2
Source datasetuspto-grants-2015_06
ORD IDord-625f1a40665a42daa41f713f925e07c9
Source noteuspto-grants-2015_06