Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1407185Generated: October 31, 2026

Nitric Acid → HCID 178468343, compound

https://huagongshe.com/reaction/1407185

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantPhosphoric AcidHCID 1004—
ReactantAcetylacetoneHCID 31261—
Reactant3-(Trifluoromethoxy)anilineHCID 73753—
ReactantPotassium AcetateHCID 517044—
ReactantSodium NitriteHCID 23668193—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 178468343HCID 17846834374%

Reaction Conditions

Temperature0 °C

Reaction Steps

3-(Trifluoromethoxy)aniline (1.00 g, 5.64 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 (389 mg, 5.64 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 mixture of potassium acetate (1.66 g, 16.92 mmol) and acetylacetone (564 mg, 5.64 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 (1.2 g, 74% yield): 1H NMR (400 MHz, CDCl3): δ ppm 2.49 (s, 3H), 2.61 (s, 3H), 7.05-7.08 (m, 1H), 7.25-7.27 (m, 11-1), 7.32 (s, 1H), 7.42 (t, J=8.0 Hz, 1H), 14.59 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916566B2
Source datasetuspto-grants-2014_12
ORD IDord-5ae95dd6bb6d459a9f8ac1bf1db4a032
Source noteuspto-grants-2014_12