HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 931176Generated: November 1, 2026
Acetoacetic Acid → 2-Acetylpyridine-4-carbonitrile
https://huagongshe.com/reaction/931176
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetoacetic Acid | HCID 96 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 4-Cyanopyridine | HCID 7506 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Ammonium Persulfate | HCID 62648 | — |
| Catalyst | Silver Nitrate | HCID 24470 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Acetylpyridine-4-carbonitrile | HCID 10464460 | 71.9% |
Reaction Steps
To a solution of isonicotinonitrile (52 g, 0.5 mol) in dichloromethane (1300 mL) and water (1100 mL) were added ammonium persulfate ((NH4)2S2O8) (170 g, 0.75 mol), silver nitrate (6.8 g, 0.04 mol) and aqueous sulfuric acid (40 mL, 98% sulfuric acid in 400 mL). A solution of 3-oxo-butyric acid (110 g, 1.25 mol) in dichloromethane (100 mL) was added dropwise while keeping the mixture refluxing. The reaction mixture was refluxed for 2 h. The resulting mixture was basified to pH˜8-9 using sodium carbonate powder. The mixture was filtered and the filtrate was extracted with dichloromethane (500 mL×3). The combined organics were dried over sodium sulfate, and concentrated under reduced pressure. The residue was recrystallized from ethanol to afford 2-acetylisonicotinonitrile (52.0 g, 71.9%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09296745B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-026b558df57d49be8331a8e3ada41600 |
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| Source note | uspto-grants-2016_03 |
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