HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 3-(6-methylpyridin-3-yl)-3-oxopropanoate → Ethyl 3-Hydroxy-3-(6-methyl-3-pyridyl)propanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| 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°. 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 nicotinoyl acetic acid ethyl ester, was 100 percent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04687856 |
| Source dataset | uspto-grants-1987_08 |
| ORD ID | ord-4a9ec14af0274134a654dea42067722b |
| Source note | uspto-grants-1987_08 |