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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 10375029 | HCID 10375029 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 3-Hydroxy-4-methyl-2-pyridinecarboxaldehyde | HCID 10329350 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05721259 |
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| Source dataset | uspto-grants-1998_02 |
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| ORD ID | ord-6edbc9498e184ab69c18a8cc29340e10 |
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| Source note | uspto-grants-1998_02 |
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