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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432793Generated: October 25, 2026

4-Fluorobenzoyl chloride → Ethyl 1-(4-fluorobenzoyl)piperidine-3-carboxylate

https://huagongshe.com/reaction/432793

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorobenzoyl chlorideHCID 67879—
ReactantEthyl nipecotateHCID 98969—
ReactantEthyl 1-benzoyl-3-piperidinecarboxylateHCID 3784394—
ProductEthyl 1-(4-fluorobenzoyl)piperidine-3-carboxylateHCID 2905457—

Reaction Steps

The reaction was run in the same manner as ethyl 1-benzoyl-3-piperidinecarboxylate, starting with ethyl nipecotate (230.9 mg; 1.47 mmol) and commercially available 4-fluorobenzoyl chloride (173 μl; 1.47 mmol). The crude product was distilled at 220° C./0.1 torr, giving ethyl 1-(4-fluorobenzoyl)-3-piperidinecarboxylate (283.4 mg) as a light yellow oil. MS m/z (positive ion) 581 (dimer+Na+; 50), 302 (M+Na+; 100), 280 (MH+; 95), 234 (45), 229 (25), 158 (50), 122.5 (60).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06664271B1
Source datasetuspto-grants-2003_12
ORD IDord-ac962e93c52747d4950d4c6c9ecd1462
Source noteuspto-grants-2003_12