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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2041308Generated: October 30, 2026

Methyl 3-methylpyridine-2-carboxylate → (3-Methylpyridin-2-yl)methanol

https://huagongshe.com/reaction/2041308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 3-methylpyridine-2-carboxylateHCID 12264487—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product(3-Methylpyridin-2-yl)methanolHCID 151436918%

Reaction Conditions

Temperature0 °C

Reaction Steps

Heat a mixture of 3-methylpicolinic acid (1.0 g, 7.3 mmol), potassium carbonate (4.1 g, 29.7 mmol), and iodomethane (4.4 g, 31.0 mmol) in acetone (35 mL) overnight under reflux. Filter, wash the residue with EtOAc, and concentrate in vacuo. Pass through a short plug of silica gel eluting with hexane/EtOAc (1:1) to provide 2-methoxycarbonyl-3-methylpyridine as a pale yellow liquid (630 mg, 57%). To a solution of 2-methoxycarbonyl-3-methylpyridine in anhydrous THF (10 mL) at 0° C., add with stirring a solution of 1M lithium aluminum hydride in THF (5 mL, 5 mmol), and continue stirring for 30 min at 0° C. Allow the mixture to warm to ambient temperature and quench cautiously with 0.5M aqueous NaOH. Heat the mixture at 60° C. for 40 min, cool to ambient temperature, extract with EtOAc, dry over anhydrous Na2SO4 and concentrate in vacuo. Purify by chromatography on silica gel eluting with hexane/EtOAc (4:3) to give the desired intermediate (90 mg, 18%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580780B2
Source datasetuspto-grants-2013_11
ORD IDord-7f0475bfc5284d44a3b79c1731f91898
Source noteuspto-grants-2013_11