HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2305258Generated: November 2, 2026
Hydrochloric Acid → Ethyl 4-(4-phenylbenzoyl)-1-piperidinecarboxylate
https://huagongshe.com/reaction/2305258
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Biphenyl | HCID 7095 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | Ethyl 4-(chlorocarbonyl)-1-piperidinecarboxylate | HCID 11096122 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | Ethyl 4-(4-phenylbenzoyl)-1-piperidinecarboxylate | HCID 18432031 | 41.5% |
Reaction Steps
A mixture of 1,1′-biphenyl (0.3 mol) and aluminum-(III)-chloride (0.6 mol) in 1,2-dichloroethane (500 ml) was stirred. A mixture of ethyl 4-(chlorocarbonyl)-1-piperidinecarboxylate (0.3 mol) in 1,2-dichloroethane (100 ml) was added dropwise over a 30-minutes period (exothermic temperature rise to 30° C.). The mixture was stirred at room temperature for 90 minutes, poured out into ice and HCl and extracted with DCM. CH3OH was added. The organic layer was separated, dried, filtered and the solvent was evaporated. The residue was purified by column chromatography over silica gel (eluent: CH2Cl2/CH3OH 99/1). The pure fractions were collected and the solvent was evaporated. The residue was crystallized from DIPE. The precipitate was filtered off and dried, yielding 42 g of ethyl 4-(4-phenylbenzoyl)-1-piperidinecarboxylate (interm. 9).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06440440B1 |
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| Source dataset | uspto-grants-2002_08 |
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| ORD ID | ord-8549dca7edad4184ace96501ca84df33 |
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| Source note | uspto-grants-2002_08 |
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