HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177874Generated: November 1, 2026
Benzenepropanoic acid → 1-(3-Phenyl-propionyl)-piperidine-4-carboxylic acid benzyl ester
https://huagongshe.com/reaction/1177874
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzenepropanoic acid | HCID 107 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Piperidinecarboxylic acid, phenylmethyl ester | HCID 11413336 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(3-Phenyl-propionyl)-piperidine-4-carboxylic acid benzyl ester | HCID 59559625 | 41.3% |
Reaction Steps
DIPEA (7 g, 9.44 mL, 54.6 mmol) was added to a stirred solution of 3-phenyl-propionic acid (3.27 g, 21.8 mmol) in DMF (15 mL). HOBT (2.94 g, 21.8 mmol) and EDCI (4.16 g, 21.8 mmol) were then added at room temperature. After 2 minutes, piperidine-4-carboxylic acid benzyl ester (4 g, 18.2 mmol) was added and the resulting mixture was stirred at room temperature overnight. Cold water was then added and the product was extracted with EtOAc and the organic layer was washed with brine. The organic phase was dried over Na2SO4 and concentrated under reduced pressure to get the residue. The obtained residue was purified by column chromatography (using 60-120 silica gel and EtOAc in hexane as eluent) to afford 2.64 g (41.25% yield) of 1-(3-phenyl-propionyl)-piperidine-4-carboxylic acid benzyl ester. LCMS Purity: 86.15%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07842696B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-50ac01976b4240d3bb12aecb60167aba |
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| Source note | uspto-grants-2010_11 |
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