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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1501206Generated: November 3, 2026

Methanol → (R)-2-oxo-1-(1-phenylethyl)-1,2-dihydropyridine-4-carboxylic acid

https://huagongshe.com/reaction/1501206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantLithium hydroxide, monohydrateHCID 168937—
Reactant(R)-methyl 2-oxo-1-(1-phenylethyl)-1,2-dihydropyridine-4-carboxylateHCID 89585124—
SolventTetrahydrofuranHCID 8028—
Product(R)-2-oxo-1-(1-phenylethyl)-1,2-dihydropyridine-4-carboxylic acidHCID 8958512380%

Reaction Conditions

Temperature20 °C

Reaction Steps

A mixture of (R)-methyl 2-oxo-1-(1-phenylethyl)-1,2-dihydropyridine-4-carboxylate (451 mg, 1.75 mmol), lithium hydroxide monohydrate (369 mg, 8.77 mmol), water (4 mL) and methanol (4 mL) in tetrahydrofuran (12 mL) was stirred at 20° C. for 12 hours. The reaction mixture was concentrated. The residue was acidified with concentrated hydrochloride solution to pH=2. The mixture was extracted with ethyl acetate (20 mL×2). The organic phase was dried over sodium sulfate and filtered. The filtrate was concentrated. The residue was purified by column chromatography (silica gel, petroleum ether/ethyl acetate=1:2) to give (R)-2-oxo-1-(1-phenylethyl)-1,2-dihydropyridine-4-carboxylic acid as a white solid (336 mg, 80%). LRMS (M+H+) m/z: calcd 243.13. found 243.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206128B2
Source datasetuspto-grants-2015_12
ORD IDord-3d6f95ffdd4345649371b01fb030891b
Source noteuspto-grants-2015_12