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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 265633Generated: October 27, 2026

O-Methylhydroxylamine → 2-Amino-6-methoxy-3-nitropyridine

https://huagongshe.com/reaction/265633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-MethylhydroxylamineHCID 4113—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Methoxy-5-nitropyridineHCID 79525—
ReactantPotassium tert-butoxideHCID 23665647—
CatalystZincchlorideHCID 3007855—
SolventDimethyl SulfoxideHCID 679—
Product2-Amino-6-methoxy-3-nitropyridineHCID 385242887%

Reaction Conditions

Temperature25 °C

Reaction Steps

6-Methoxy-3-nitropyridine (154 mg, 1 mmol) and O-methylhydroxylamine (71 mg, 1.5 mmol) were dissolved in DMSO (2 ml), and a resulting solution was added dropwise to a DMSO solution (3 ml) containing potassium tert-butoxide (336 mg, 3 mmol) and zinc (II) chloride (136 mg, 1 mmol) at 25° C. After completion of the addition, the resulting mixture was stirred at 25 ° C. for 9 hours and an aqueous saturated ammonium chloride solution (50 ml) was added, followed by extraction with ethyl acetate (80 ml). A resulting organic layer was dried over anhydrous magnesium sulfate, and then isolated and purified by subjection to silica gel thin layer chromatography [eluent: ethyl acetate/hexane=1/1] to obtain 147 mg of 2-amino-6-methoxy-3-nitropyridine (yield: 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05648496
Source datasetuspto-grants-1997_07
ORD IDord-e2e437f90535462b87ba39f110724f13
Source noteuspto-grants-1997_07