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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696787Generated: October 26, 2026

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

https://huagongshe.com/reaction/1696787

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorobenzoyl chlorideHCID 67879—
ReactantDiisopropylethylamineHCID 81531—
ReactantEthyl nipecotateHCID 98969—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 1-(4-fluorobenzoyl)piperidine-3-carboxylateHCID 290545733%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of Ethyl nipecotate (2 g, 12.72 mmol) in THF (25 ml, 0.5M) was added DIEA (4.79 ml, 27.99 mmol). The reaction mixture was cooled to 0° C. and 4-Fluoro-benzoyl chloride (2.5 g-15.76 mmol) was slowly added. The reaction was to go up to R.T and stirred for 24 h. The solution was concentrated and DCM was added following by HCl 1N. The aqueous phase was separated and organic phase was extracted twice with HCl 1N and twice with water, dried over Na2SO4, filtered and concentrated to afford 1.15 g (33%) of 1-(4-Fluoro-benzoyl)-piperidine-3-carboxylic acid ethyl ester as a colorless oil which can be used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163775B2
Source datasetuspto-grants-2012_04
ORD IDord-65424744911e48a687cc1fd229a0bf6e
Source noteuspto-grants-2012_04