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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414759Generated: October 26, 2026

Sodium Carbonate → 2-Methyl-4-amino-5-pyrimidine aldoxime

https://huagongshe.com/reaction/414759

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant4-Amino-2-methylpyrimidine-5-carbaldehydeHCID 12904726—
SolventMethanolHCID 887—
Product2-Methyl-4-amino-5-pyrimidine aldoximeHCID 8557148982.3%

Reaction Steps

To a mixture of 8.6 g of 2-methyl-4-amino-5-formylpyrimidine and 340 ml of methanol, while stirring at room temperature, was added dropwise gradually 40 ml of an aqueous solution of 5.20 g of hydroxylamine hydrochloride and 7.80 g of sodium carbonate. As the reaction proceeded, crystals precipitated. Four hours later, the crystals were collected by filtration, washed with methanol and water, followed by drying under reduced pressure to give 7.84 g (82.3%) of 2-methyl-4-amino-5-pyrimidine aldoxime. The mother liquor was subjected to high performance liquid chromatography to quantitatively determine 2-methyl-4-amino-5-pyrimidine aldoxime (by absolute calibration curve method) to confirm that 1.41 g (14.8%) of the object compound was produced. The total yield of the crystals and the object compound in the mother liquor was 97.1%. The mother liquor was concentrated to dryness under reduced pressure, followed by recrystallization from a mixture solvent of methanol/ether to isolate 0.8 g of 2-methyl-4-amino-5-pyrimidine aldoxime.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04794182
Source datasetuspto-grants-1988_12
ORD IDord-21b53de72e954b6d95ed91b21548e2c9
Source noteuspto-grants-1988_12