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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Fluoro-2-iodobenzene | HCID 67673 | — |
| Reactant | Ethyl 4-piperidinecarboxylate | HCID 70770 | — |
| Reactant | L-Proline | HCID 145742 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(2-Fluorophenyl)piperidine-4-carboxylic acid ethyl ester | HCID 58563729 | 26% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07985755B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-1d1dc6078b3240d1a2586881711ffc03 |
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| Source note | uspto-grants-2011_07 |
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