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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1895189Generated: October 27, 2026

Nitric Acid → HCID 178468322, compound

https://huagongshe.com/reaction/1895189

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantPhosphoric AcidHCID 1004—
ReactantAcetylacetoneHCID 31261—
Reactant2-(1-Methylethoxy)benzenamineHCID 34436—
ReactantPotassium AcetateHCID 517044—
ReactantSodium NitriteHCID 23668193—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 178468322HCID 17846832230.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-(1-Methylethoxy)aniline (1.00 g, 6.62 mmol) was added to a solution of 6 mL of phosphoric acid (85%) and 4 mL of nitric acid (65%) at −6° C., followed by sodium nitrite (0.55 g, 7.95 mmol) in 2 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 (1.95 g, 19.86 mmol) and acetylacetone (0.86 g, 8.61 mmol) in 40 mL of ethanol and 10 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 (0.53 g, 30% yield): 1H NMR (400 MHz, CDCl3): δ ppm 1.28-1.41 (6H, m), 2.50 (3H, s), 2.63 (3H, s), 4.53-4.59 (1H, m), 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 numberUS08513251B2
Source datasetuspto-grants-2013_08
ORD IDord-a7b94aac8f1743f4bab3f352e48d0ff0
Source noteuspto-grants-2013_08