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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1805539Generated: October 29, 2026

Nitric Acid → HCID 178468315, compound

https://huagongshe.com/reaction/1805539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantPhosphoric AcidHCID 1004—
ReactantAcetylacetoneHCID 31261—
Reactant2-AminobenzonitrileHCID 72913—
ReactantPotassium AcetateHCID 517044—
ReactantSodium NitriteHCID 23668193—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 178468315HCID 17846831541.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-Aminobenzonitrile (5.00 g, 42.37 mmol) was added to a solution of 30 mL of phosphoric acid (85%) and 20 mL of nitric acid (65%) at −6° C., followed by sodium nitrite (3.50 g, 50.78 mmol) in 10 mL of water dropwise at 0° C., and the mixture was stirred at 0° C. for 30 min. Then, to the reaction mixture was added dropwise a solution of potassium acetate (12.45 g, 127.11 mmol) and acetylacetone (5.51 g, 55.08 mmol) in 80 mL of ethanol and 48 mL of water. The mixture was stirred at room temperature overnight, filtered, washed with water, EtOH/H2O (1/1) and hexane, and dried to give the title compound (4.00 g, 41% yield): 1H NMR (400 MHz, CDCl3): δ ppm 2.50 (3H, s), 2.63 (3H, s), 7.21-7.25 (1H, m), 7.62-7.66 (2H, m), 7.77-7.79 (1H, m), 15.01 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354411B2
Source datasetuspto-grants-2013_01
ORD IDord-02955077bac14e90828a86199dae1247
Source noteuspto-grants-2013_01