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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1805493Generated: November 4, 2026

Nitric Acid → HCID 178496287, compound

https://huagongshe.com/reaction/1805493

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantPhosphoric AcidHCID 1004—
Reactant4-AminopyridineHCID 1727—
ReactantMethyl 4-methoxyacetoacetateHCID 123500—
ReactantSodium AcetateHCID 517045—
ReactantSodium NitriteHCID 23668193—
SolventMethanolHCID 887—
ProductHCID 178496287HCID 17849628719%

Reaction Conditions

Temperature-6 °C

Reaction Steps

4-Aminopyridine (3.6 g, 38 mmol) was added to a mixture of phosphoric acid (10 mL, 150 mmol) and nitric acid (5 mL, 78 mmol) at −6° C. Sodium nitrite (3.2 g, 46 mmol) was added portionwise to the mixture at −6° C., and then crushed ice (ca. 25 g) was added into the solution. After stirring at −6° C. for 10 min, the mixture was poured into a suspension of methyl 4-methoxyacetoacetate (5.0 mL, 38 mmol) and sodium acetate (44 g, 540 mmol) in MeOH (100 mL) at 0° C. The mixture was partitioned between AcOEt and water. The aqueous layer was extracted with AcOEt. The combined organic extract was washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The residual solid was washed with AcOEt/hexane (1/3) to give the title compound (1.8 g, 19% yield) as a yellow solid: 1H NMR (300 MHz, CDCl3): δ ppm 3.48-3.53 (3H, m), 3.89-3.95 (3H, m), 4.64-4.69 (2H, m), 7.17-7.34 (2H, m), 8.54-8.60 (2H, m), 12.65 (1H, brs).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354411B2
Source datasetuspto-grants-2013_01
ORD IDord-0bc60fccca1e4a579a865035dca6660b
Source noteuspto-grants-2013_01