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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727844Generated: October 30, 2026

Pyridine → 4-[1-(1-Imidazolyl)-butyl]-benzonitrile

https://huagongshe.com/reaction/727844

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantPotassium CarbonateHCID 11430—
Reactant4-[1-(1-Imidazolyl)-butyl]-benzamideHCID 14514367—
Solvent1,4-DioxaneHCID 31275—
Product4-[1-(1-Imidazolyl)-butyl]-benzonitrileHCID 1451436270.5%

Reaction Conditions

Temperature5 °C

Reaction Steps

4.9 g of the amide of example 3 is dissolved in 50 ml of dioxane and 3.23 ml of pyridine and mixed with 3.16 ml of trifluoroacetic acid anhydride under ice cooled at 5° C. internal temperature. After 20 hours of stirring at room temperature it is added to half-saturated potassium carbonate solution, extracted with ether and the ether phase is dried and concentrated by evaporation. After distillation on a bulb tube at 200°-215° C./0.05 mbar, 3.2 g of 4-[1-(1-imidazolyl)-butyl]-benzonitrile is obtained, which, after crystallization from ether, melts at 63°-71° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05045558
Source datasetuspto-grants-1991_09
ORD IDord-958aeea9d15a41b1bd57817014b6bf38
Source noteuspto-grants-1991_09