HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167652Generated: October 25, 2026
Ethyl isonicotinate → 2-Cyano-2-[4-(1,1-dimethylethyl)phenyl]-1-(4-pyridyl)ethanone
https://huagongshe.com/reaction/1167652
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl isonicotinate | HCID 15291 | — |
| Reactant | (4-tert-Butylphenyl)acetonitrile | HCID 76784 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 2-Cyano-2-[4-(1,1-dimethylethyl)phenyl]-1-(4-pyridyl)ethanone | HCID 22993744 | 35% |
Reaction Steps
To a solution of ethyl isonicotinate (12 g) and 4-(1,1-Dimethylethyl)phenylacetonitrile (9.1 g) in tert-butyl alcohol (36 mL), was added potassium tert-butoxide (7.3 g), and the mixture was stirred at 100° C. for 3 h. After cooling, the resulting mixture was dissolved in water and washed with isopropyl ether. The aqueous phase was adjusted to pH 7.0 with 2 N hydrochloric acid and extracted with ethyl acetate. The extract was washed with water, dried, and the solvent was evaporated. The crystalline residue was recrystallized from ethyl acetate-isopropyl ether to obtain 2-cyano-2-[4-(1,1-dimethylethyl)phenyl]-1-(4-pyridyl)ethanone (5.09 g, yield 35%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06620825B1 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-c388df1a2ee94b51a832892f3e659873 |
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| Source note | uspto-grants-2003_09 |
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