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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491660Generated: October 31, 2026

Nitric Acid → 4-(2-Methylamino-pyrimidin-4-yloxy)-2-nitro-phenol

https://huagongshe.com/reaction/491660

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantSodium BicarbonateHCID 516892—
Reactant4-(2-Methylamino-pyrimidin-4-yloxy)-phenolHCID 17756598—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product4-(2-Methylamino-pyrimidin-4-yloxy)-2-nitro-phenolHCID 17755014—

Reaction Steps

4-(2-Methylamino-pyrimidin-4-yloxy)-phenol (Step C, 0.20 g, 0.92 mmol) was dissolved in 5 mL AcOH at RT. Fuming HNO3 (0.064 g, 0.92 mmol) was diluted with about 0.012 mL water, then added dropwise over 1 min to the reaction. The reaction was stirred for 18 h, after which it was added slowly to 40 mL saturated aqueous NaHCO3 and extracted with CH2Cl2. The organic layer was washed with NaHCO3 and brine, dried over Na2SO4, filtered, and concentrated in vacuo. The crude residue was purified by silica gel column chromatography using hexanes/EtOAc gradient to yield the title compound. MS (MH+)=263.1; Calc'd 262.23 for C11H10N4O4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531553B2
Source datasetuspto-grants-2009_05
ORD IDord-860a34310c3c4f4bafee8a4b3b21e69e
Source noteuspto-grants-2009_05