HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1689902Generated: October 31, 2026
Water → Ethyl 1-benzylpiperidine-4-carboxylate
https://huagongshe.com/reaction/1689902
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 4-piperidinecarboxylate | HCID 70770 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Ethyl 1-benzylpiperidine-4-carboxylate | HCID 90423 | — |
Reaction Steps
Amine preparation: To a solution of piperidine-4-carboxylic acid ethyl ester (3.0 g) stirring in dry MeCN (30 mL) was added potassium carbonate (2.90 g) followed by benzyl bromide (2.5 mL). The mixture was warmed to 78° C. After 3 h the mixture was cooled, poured into water (100 mL) and extracted into ethyl acetate, dried (MgSO4) and the solvent removed in vacuo. The residue was purified using flash chromatography to give 1-benzyl-piperidine-4-carboxylic acid ethyl ester (2.17 g) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08153629B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-9f23ba576b7148b08327354b408a7608 |
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| Source note | uspto-grants-2012_04 |
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