HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 3928Generated: October 25, 2026
Ethyl 3-(6-methylpyridin-3-yl)-3-oxopropanoate → Ethyl 3-Hydroxy-3-(6-methyl-3-pyridyl)propanoate
https://huagongshe.com/reaction/3928
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl 3-(6-methylpyridin-3-yl)-3-oxopropanoate | HCID 89013 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 3-Hydroxy-3-(6-methyl-3-pyridyl)propanoate | HCID 14178170 | — |
Reaction Steps
10.0 g (0.048 mol) of 6-methyl nicotinoyl acetic acid ethyl ester (distilled) was dissolved in 200 ml of 95 percent ethanol, mixed with 1 g of 5 percent palladium on activated carbon and poured into a 1-liter autoclave. The autoclave was put under 10 bars of hydrogen and stirred at 20° C. The hydrogenation ended after 6 hours. The autoclave was opened, and the reaction solution filtered and evaporated. 10.0 g of 3-hydroxy-3-(2-methyl-5-pyridyl)-propionic acid ethyl ester remained, which according to NMR and DC was pure. The yield, in relation to the 6-methyl nicotinyl acetic acid ethyl ester, was 100 percent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04723017 |
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| Source dataset | uspto-grants-1988_02 |
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| ORD ID | ord-f2864fc6aa97413c9046a412cd850dc6 |
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| Source note | uspto-grants-1988_02 |
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