Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577583Generated: October 30, 2026

Methyl 5-(benzyloxy)-3-methyl-2-(propan-2-yloxy)pyridine-4-carboxylate → Methyl 5-hydroxy-3-methyl-2-(propan-2-yloxy)pyridine-4-carboxylate

https://huagongshe.com/reaction/577583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 5-(benzyloxy)-3-methyl-2-(propan-2-yloxy)pyridine-4-carboxylateHCID 86723809—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductMethyl 5-hydroxy-3-methyl-2-(propan-2-yloxy)pyridine-4-carboxylateHCID 8672381089%

Reaction Steps

A mixture of methyl 5-(benzyloxy)-3-methyl-2-(propan-2-yloxy)pyridine-4-carboxylate (131b, 1.1 g, 3.5 mmol) and Pd/C (0.5 g) in MeOH (60 mL) was hydrogenated under an H2 balloon at room temperature for 2 hours. The reaction mixture was filtered through CELITE® and the filtrate was concentrated under vacuum to give methyl 5-hydroxy-3-methyl-2-(propan-2-yloxy)pyridine-4-carboxylate (131c, 0.7 g, 89%) as yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040515B2
Source datasetuspto-grants-2015_05
ORD IDord-19c2cda567c54fc3a5de55ee58b37858
Source noteuspto-grants-2015_05