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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015366Generated: October 29, 2026

Potassium Carbonate → 1-(2-Fluorophenyl)piperidine-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1015366

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-Fluoro-2-iodobenzeneHCID 67673—
ReactantEthyl 4-piperidinecarboxylateHCID 70770—
ReactantL-ProlineHCID 145742—
CatalystCopper iodideHCID 83717—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product1-(2-Fluorophenyl)piperidine-4-carboxylic acid ethyl esterHCID 5856372926%

Reaction Conditions

Temperature90 °C

Reaction Steps

1-Fluoro-2-iodobenzene (0.58 mL, 5.0 mmol) was added to a mixture of ethyl isonipecotate (1.2 mL, 7.5 mmol), potassium carbonate (1.4 g, 10 mmol), L-proline (0.12 g, 1 mmol) and copper iodide (0.095 g, 0.5 mmol) in 4 mL of dimethyl sulfoxide. Reaction stirred at 90° C. for 48 hours. The mixture was poured into a water (40 mL) solution and extracted with ethyl acetate (EtOAc) (4×10 mL). The combined organic layers were washed with brine (40 mL) and dried over anhydrous Na2SO4. The organic layer was concentrated in vacuo to obtain the crude mixture, which was purified by silica gel flash chromatography, using EtOAc/hexane (gradient system), to obtain 1-(2-fluorophenyl)piperidine-4-carboxylic acid ethyl ester (0.325 g, 26% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985755B2
Source datasetuspto-grants-2011_07
ORD IDord-1d1dc6078b3240d1a2586881711ffc03
Source noteuspto-grants-2011_07