Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 931176Generated: November 1, 2026

Acetoacetic Acid → 2-Acetylpyridine-4-carbonitrile

https://huagongshe.com/reaction/931176

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoacetic AcidHCID 96—
ReactantSulfuric AcidHCID 1118—
Reactant4-CyanopyridineHCID 7506—
ReactantSodium CarbonateHCID 10340—
ReactantAmmonium PersulfateHCID 62648—
CatalystSilver NitrateHCID 24470—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2-Acetylpyridine-4-carbonitrileHCID 1046446071.9%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296745B2
Source datasetuspto-grants-2016_03
ORD IDord-026b558df57d49be8331a8e3ada41600
Source noteuspto-grants-2016_03