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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508583Generated: October 28, 2026

3-Hydroxypyridine → HCID 178505469, compound

https://huagongshe.com/reaction/508583

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxypyridineHCID 7971—
ReactantPotassium HydroxideHCID 14797—
ReactantSodium HydroxideHCID 14798—
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 178519719HCID 178519719—
SolventPyridineHCID 1049—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178505469HCID 17850546910.2%

Reaction Steps

The compound of Example 1 (150 mg) was dissolved in THF (5 mL), and thionyl chloride (60 mg) and pyridine (146 mg) were added thereto. The mixture was stirred for 30 minutes at room temperature, and then 3-hydroxypyridine (87 mg) and potassium hydroxide (65 mg) were added thereto. The mixture was heated to reflux for 30 minutes while being stirred. A 10% aqueous solution of sodium hydroxide was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was washed with saturated brine and then dried over anhydrous sodium sulfate. After distilling off the solvent under reduced pressure, the residue was purified by silica gel column chromatography (60% to 100% ethyl acetate/hexane), and thus the title compound (19 mg) was obtained as a yellow amorphous material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096531B2
Source datasetuspto-grants-2015_08
ORD IDord-e5e7932b8e6b44d1a8cbd50696bbfaa1
Source noteuspto-grants-2015_08