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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1805549Generated: November 1, 2026

Nitric Acid → HCID 178468351, compound

https://huagongshe.com/reaction/1805549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantPhosphoric AcidHCID 1004—
ReactantSodium CarbonateHCID 10340—
ReactantAcetylacetoneHCID 31261—
ReactantPotassium AcetateHCID 517044—
Reactant4-(4-Methylpiperazin-1-yl)anilineHCID 737253—
ReactantSodium NitriteHCID 23668193—
SolventEthanolHCID 702—
ProductHCID 178468351HCID 17846835139%

Reaction Conditions

Temperature-6 °C

Reaction Steps

4-(4-Methylpiperazin-1-yl)aniline (1000 mg, 5.24 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 sodium nitrite (361 mg, 5.24 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 (524 mg, 5.24 mmol) and potassium acetate (30 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 (610 mg, 39% yield): 1H NMR (400 MHz, CDCl3): δ ppm 2.40 (3H, s), 2.50 (3H, s), 2.62 (3H, s), 3.10 (4H, t, J=5.2 Hz), 3.25 (4H, t, J=4.8 Hz), 7.30 (2H, d, J=8.8 Hz), 7.37 (2H, d, J=7.6 Hz), 15.08 (1H, brs).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354411B2
Source datasetuspto-grants-2013_01
ORD IDord-d3f6cf6ac4b2476ca1379a1cc55e73cc
Source noteuspto-grants-2013_01