HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 501818Generated: October 31, 2026
Ethanol → Ethyl 5-(hydroxymethyl)pyridine-2-carboxylate
https://huagongshe.com/reaction/501818
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 5-(Ethoxycarbonyl)pyridine-2-carboxylic acid | HCID 592087 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Calcium Chloride | HCID 5284359 | — |
| Product | Ethyl 5-(hydroxymethyl)pyridine-2-carboxylate | HCID 13518564 | — |
Reaction Steps
0.636 g of sodium borohydride was added to 22 mL of ice-cooled ethanol, to which a solution of 1.09 g of calcium chloride in 14 mL of ethanol was added dropwise, followed by addition of 1.20 g of 5-(ethoxycarbonyl)-2-pyridinecarboxylic acid ½ calcium salt, and this mixture was stirred for one hour at room temperature. The reaction mixture, to which 2.8 mL of concentrated sulfuric acid was added, was stirred for 6 hours while heating it under reflux. The reaction mixture was cooled to room temperature and concentrated under reduced pressure followed by successive addition of a saturated aqueous solution of sodium hydrogen carbonate and chloroform, and then the organic phase was separated therefrom. The resultant organic phase was washed with a saturated sodium chloride solution and dried over anhydrous magnesium sulfate, and the solvent was distilled out under reduced pressure to yield 0.34 g of ethyl 5-(hydroxymethyl)-2-pyridinecarboxylate as light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07772285B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-8aea6389fda448f4b9bb5069139d32a6 |
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| Source note | uspto-grants-2010_08 |
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