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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | Ethyl 1-(5-fluoropyridin-2-yl)piperidine-4-carboxylate | HCID 58302994 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(5-Fluoropyridin-2-yl)piperidine-4-carboxylic acid | HCID 58303118 | 87% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09226916B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-44e9136703e540d39c8bdc50d13226f6 |
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| Source note | uspto-grants-2016_01 |
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