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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-(6-methylpyridin-3-yl)-3-oxopropanoateHCID 89013—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductEthyl 3-Hydroxy-3-(6-methyl-3-pyridyl)propanoateHCID 14178170—

Reaction Conditions

Temperature20 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04723017
Source datasetuspto-grants-1988_02
ORD IDord-f2864fc6aa97413c9046a412cd850dc6
Source noteuspto-grants-1988_02