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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019034Generated: October 31, 2026

Pyridine → pentafluorophenyl 5-[(E)-3-(imidazol-1-yl)prop-1-en-1-yl]-2-(4-fluorophenethyl)benzoate

https://huagongshe.com/reaction/1019034

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPentafluorophenyl TrifluoroacetateHCID 4327891—
Reactant5-[3-(Imidazol-1-yl)prop-1-en-1-yl]-2-(4-fluorophenethyl)benzoic acidHCID 54510653—
SolventDimethylformamideHCID 6228—
Productpentafluorophenyl 5-[(E)-3-(imidazol-1-yl)prop-1-en-1-yl]-2-(4-fluorophenethyl)benzoateHCID 18399494—
Productpentafluorophenyl 5-[(Z)-3-(imidazol-1-yl)prop-1-en-1-yl]-2-(4-fluorophenethyl)benzoateHCID 86758617—

Reaction Steps

Pentafluorophenyl trifluoroacetate (1.47 ml; 8.6 mmol) was added to a solution of 5-[3-(imidazol-1-yl)prop-1-en-1-yl]-2-(4-fluorophenethyl)benzoic acid (2.5 g, 7.14 mmol) and pyridine (0.7 ml; 8.6 mmol) in DMF (7 ml). After stirring at ambient temperature overnight, the mixture was evaporated to dryness and the residue extracted with ethyl acetate, washed with saturated sodium hydrogen carbonate solution and saturated brine. After evaporation the reaction mixture was purified by flash chromatography, eluting with dichloromethane/ethanol (99/1) to give E isomer pentafluorophenyl 5-[(E)-3-(imidazol-1-yl)prop-1-en-1-yl]-2-(4-fluorophenethyl)benzoate and Z isomer pentafluorophenyl 5-[(Z)-3-(imidazol-1-yl)prop-1-en-1-yl]-2-(4-fluorophenethyl)benzoate. Yield: 68%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06486156B1
Source datasetuspto-grants-2002_11
ORD IDord-51e20c7c773e4b4c8d36a1aa8f7c16b1
Source noteuspto-grants-2002_11