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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1624552Generated: November 1, 2026

Sulfuric Acid → HCID 178468354, compound

https://huagongshe.com/reaction/1624552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactant3-AminopyridineHCID 10009—
ReactantSodium CarbonateHCID 10340—
ReactantAcetylacetoneHCID 31261—
ReactantPotassium AcetateHCID 517044—
ReactantSodium NitriteHCID 23668193—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 178468354HCID 17846835420%

Reaction Steps

To 3-aminopyridine (564 mg, 6.00 mmol) were added 4 mL of concentrated sulfuric acid and 1.2 mL of water at 0° C., and the mixture was stirred at room temperature until it was clear. To the reaction mixture was added a solution of sodium nitrite (414 mg, 6.00 mmol) in water (1.2 mL) at 0° C. The mixture was stirred for several min (>15 min). The solution of diazonium salt was poured into the solution of 2,4-pentanedione (600 mg, 6.00 mmol) and potassium acetate (18.0 g, 180 mmol) in ethanol (120 mL) at 0° C. The mixture was stirred at 0° C. for 30 min and at room temperature for 30 min. The reaction mixture was added to 120 mL of saturated Na2CO3 aqueous solution. The mixture was extracted with dichloromethane, washed with water and brine, dried over Na2SO4, and concentrated under reduced pressure to give 3-(pyridin-3-ylhydrazono)pentane-2,4-dione (242 mg, yield 20%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778944B2
Source datasetuspto-grants-2014_07
ORD IDord-f7636db26e164e9792420873acbee607
Source noteuspto-grants-2014_07