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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018990Generated: November 1, 2026

Ethyl 1-benzylpiperidine-4-carboxylate → HCID 18399772, compound

https://huagongshe.com/reaction/1018990

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 1-benzylpiperidine-4-carboxylateHCID 90423—
ReactantThiopheneethanamineHCID 116521—
ReactantSodiumHCID 5360545—
SolventEthanolHCID 702—
ProductHCID 18399772HCID 18399772—

Reaction Steps

22.15 g of ethyl 1-benzyl-4-piperidinecarboxylate and 1 equivalent of the product obtained in Step B are added to a solution of 4.12 g of sodium in 103 ml of anhydrous ethanol. After 12 hours' reaction at reflux, the reaction mixture is evaporated. The residue is taken up in dichloromethane and washed with water, and then the organic phase is dried, filtered and evaporated, enabling an oil to be obtained which crystallises in diisopropyl ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06486171B2
Source datasetuspto-grants-2002_11
ORD IDord-c7b5ca28d86a441295edbcb9b0cfd004
Source noteuspto-grants-2002_11