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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368481Generated: October 30, 2026

(E)-ethyl 1-(4-fluorophenyl)-2-(2,3,6-trifluorostyryl)-1H-imidazole-5-carboxylate → ethyl 1-(4-fluorophenyl)-2-(2,3,6-trifluorophenethyl)-1H-imidazole-5-carboxylate

https://huagongshe.com/reaction/2368481

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(E)-ethyl 1-(4-fluorophenyl)-2-(2,3,6-trifluorostyryl)-1H-imidazole-5-carboxylateHCID 86677544—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Productethyl 1-(4-fluorophenyl)-2-(2,3,6-trifluorophenethyl)-1H-imidazole-5-carboxylateHCID 71117630—

Reaction Steps

To a solution of (E)-ethyl 1-(4-fluorophenyl)-2-(2,3,6-trifluorostyryl)-1H-imidazole-5-carboxylate (17) (60 mg, 0.16 mmol) in ethanol (10 mL) was added Pd/C (10% Degussa type, 10 mg). A balloon of hydrogen gas was attached and the reaction was evacuated and back-filled with hydrogen three times. The reaction was stirred under a hydrogen balloon overnight at room temperature, filtered through a pad of celite and concentrated in vacuo to give ethyl 1-(4-fluorophenyl)-2-(2,3,6-trifluorophenethyl)-1H-imidazole-5-carboxylate (18).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703776B2
Source datasetuspto-grants-2014_04
ORD IDord-245574b65d6940239e854900befb44cc
Source noteuspto-grants-2014_04