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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587394Generated: October 27, 2026

Acetic Acid → 1-(5-Fluoropyridin-2-yl)piperidine-4-carboxylic acid

https://huagongshe.com/reaction/587394

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantEthyl AcetateHCID 8857—
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantEthyl 1-(5-fluoropyridin-2-yl)piperidine-4-carboxylateHCID 58302994—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1-(5-Fluoropyridin-2-yl)piperidine-4-carboxylic acidHCID 5830311887%

Reaction Conditions

Temperature20 °C

Reaction Steps

A mixture of 4 g (16 mmol) 5′-Fluoro-3,4,5,6-tetrahydro-2H-[1,2′]bipyridinyl-4-carboxylic acid ethyl ester and 0.832 g (20 mmol) LiOH.H2O in 50 mL THF, 50 mL water and 5 mL methanol was stirred for 2 h at 20° C. Acetic acid was added to pH 6 and water and ethyl acetate. The mixture was extracted with ethyl acetate and the combined organic layers were washed with brine, dried with Na2SO4, filtered and evaporated to dryness. The residue was purified by column chromatography on silica eluting with a gradient formed from heptane and ethyl acetate. The product containing fractions were evaporated to yield 3.1 g (87%) of the title compound as off-white solid. MS m/e: 223.1 [M−H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09226916B2
Source datasetuspto-grants-2016_01
ORD IDord-44e9136703e540d39c8bdc50d13226f6
Source noteuspto-grants-2016_01