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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 863573Generated: October 29, 2026

HCID 10375029, compound → 3-Hydroxy-4-methyl-2-pyridinecarboxaldehyde

https://huagongshe.com/reaction/863573

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 10375029HCID 10375029—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
SolventSulfuric AcidHCID 1118—
Product3-Hydroxy-4-methyl-2-pyridinecarboxaldehydeHCID 10329350—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-(1,3-dioxolanyl)-4-methyl-3-aminopyridine (0.60 g, 3.3 mmol) in 15 mL of 10% H2SO4 at 0° C. (ice bath) with stirring was added dropwise a solution of NaNO2 (0.38 g, 5.5 mmol) in 3 mL of water. The mixture was stirred at 0° C. for 15 min and then heated in a steam-bath for 30 min. The resulting solution was evaporated at room temperature under reduced pressure to yield 3-hydroxy-4-methyl-2-formylpyridine as a syrup, which was dissolved in 15 mL of water, decolorized with charcoal and filtered. To the filtrate was added a solution of thiosemicarbazide (0.31 g, 3.3 mmol) in 5 mL of 5% HCl. The mixture was refluxed for 30 min, cooled and the yellow precipitate was filtered, washed with water, and recrystallized from aqueous ethanol solution (1:1, v/v) containing 5% conc. HCl to afford 0.21 g (30%) of product: the mp and all spectroscopic data were identical with those obtained in Example XLIII.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05721259
Source datasetuspto-grants-1998_02
ORD IDord-6edbc9498e184ab69c18a8cc29340e10
Source noteuspto-grants-1998_02