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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1407186Generated: October 29, 2026

Nitric Acid → HCID 178474263, compound

https://huagongshe.com/reaction/1407186

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantPhosphoric AcidHCID 1004—
ReactantSodium CarbonateHCID 10340—
Reactant4-AminoacetanilideHCID 31230—
ReactantAcetylacetoneHCID 31261—
ReactantPotassium AcetateHCID 517044—
ReactantSodium NitriteHCID 23668193—
SolventEthanolHCID 702—
ProductHCID 178474263HCID 17847426380.5%

Reaction Conditions

Temperature-6 °C

Reaction Steps

N-(4-Aminophenyl)acetamide (1000 mg, 6.66 mmol) was added to a solution of 6 mL of phosphoric acid (85%) and 4 mL of nitric acid (65%) at −6° C. When the mixture reached to room temperature, it was cooled to −6° C. and solid sodium nitrite (460 mg, 6.66 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 (666 mg, 6.66 mmol) and potassium acetate (40 g) in ethanol (400 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 (1400 mg, 80% yield): 1H NMR (400 MHz, CDCl3): δ ppm 2.22 (3H, s), 2.48 (3H, s), 2.60 (3H, s), 7.22 (1H, brs), 7.38 (2H, d, J=8.8 Hz), 7.57 (2H, d, J=8.8 Hz), 14.84 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916566B2
Source datasetuspto-grants-2014_12
ORD IDord-d26c3ec8410242a7862aa3bdd0e7c7db
Source noteuspto-grants-2014_12