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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1624669Generated: October 31, 2026

Nitric Acid → HCID 178468353, compound

https://huagongshe.com/reaction/1624669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantPhosphoric AcidHCID 1004—
ReactantSodium CarbonateHCID 10340—
ReactantAcetylacetoneHCID 31261—
ReactantPotassium AcetateHCID 517044—
Reactant4-(1,2,4-Triazol-1-yl)anilineHCID 735826—
ReactantSodium NitriteHCID 23668193—
SolventEthanolHCID 702—
ProductHCID 178468353HCID 17846835371%

Reaction Conditions

Temperature-6 °C

Reaction Steps

4-(1H-1,2,4-Triazol-1-yl)aniline (500 mg, 3.12 mmol) was added to a solution of 3 mL of phosphoric acid (85%) and 2 mL of nitric acid (65%) at −6° C. When the mixture reached to room temperature, it was cooled to −6° C. and sodium nitrite (216 mg, 3.12 mmol) was added during 10 min. Small piece of ice (50 g) was added into the solution. The mixture was added at 0° C. to a suspension of 2,4-pentanedione (312 mg, 3.12 mmol) and potassium acetate (20 g) in ethanol (250 mL). The solution was stirred for 15 min, and then was added to 250 mL of saturated Na2CO3 aqueous solution, extracted with dichloromethane, washed with water and brine, dried over Na2SO4, and concentrated under reduced pressure to give the title compound (600 mg, 71% yield) as a brown solid: 1H NMR (400 MHz, CDCl3): δ ppm 2.54 (3H, s), 2.63 (3H, s), 7.55 (2H, d, J=8.8 Hz), 7.74 (2H, d, J=8.8 Hz), 8.12 (1H, s), 8.54 (1H, s), 14.76 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778944B2
Source datasetuspto-grants-2014_07
ORD IDord-457178eabaee46c88f2cb54901b629e6
Source noteuspto-grants-2014_07