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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-[1-(1-Imidazolyl)-butyl]-benzamide | HCID 14514367 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-[1-(1-Imidazolyl)-butyl]-benzonitrile | HCID 14514362 | 70.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05045558 |
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| Source dataset | uspto-grants-1991_09 |
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| ORD ID | ord-958aeea9d15a41b1bd57817014b6bf38 |
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| Source note | uspto-grants-1991_09 |
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