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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBiphenylHCID 7095—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantEthyl 4-(chlorocarbonyl)-1-piperidinecarboxylateHCID 11096122—
Solvent1,2-DichloroethaneHCID 11—
ProductEthyl 4-(4-phenylbenzoyl)-1-piperidinecarboxylateHCID 1843203141.5%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06440440B1
Source datasetuspto-grants-2002_08
ORD IDord-8549dca7edad4184ace96501ca84df33
Source noteuspto-grants-2002_08