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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368499Generated: November 1, 2026

Water → ethyl 2-((2-chloro-6-fluorobenzyl)oxy)-1-(4-fluorophenyl)-1H-imidazole-5-carboxylate

https://huagongshe.com/reaction/2368499

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant2-Chloro-6-fluorobenzyl alcoholHCID 91868—
Reactantethyl 1-(4-fluorophenyl)-2-iodo-1H-imidazole-5-carboxylateHCID 71117744—
SolventTetrahydrofuranHCID 8028—
Productethyl 2-((2-chloro-6-fluorobenzyl)oxy)-1-(4-fluorophenyl)-1H-imidazole-5-carboxylateHCID 71117954—

Reaction Steps

To a solution of (2-chloro-6-fluorophenyl)methanol (160.5 mg, 0.99 mmol) in THF (8 mL) was added sodium hydride (40 mg, 0.99 mmol) and the reaction was stirred at room temperature. After 25 minutes ethyl 1-(4-fluorophenyl)-2-iodo-1H-imidazole-5-carboxylate (38) (300 mg, 0.83 mmol) was added and the reaction was refluxed overnight. Water was added slowly and the solution was extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo to afford ethyl 2-((2-chloro-6-fluorobenzyl)oxy)-1-(4-fluorophenyl)-1H-imidazole-5-carboxylate (39).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703776B2
Source datasetuspto-grants-2014_04
ORD IDord-49b64bd782894b0995c857b2d6069e39
Source noteuspto-grants-2014_04