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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241012Generated: October 29, 2026

Piperidine → Ethyl 4-(piperidin-1-yl)butanoate

https://huagongshe.com/reaction/241012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantButanoic acid, 3-bromo-, ethyl esterHCID 95424—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductEthyl 4-(piperidin-1-yl)butanoateHCID 1404435681.2%

Reaction Steps

To a solution of ethyl 3-bromobutanoate (6.0 mL, 42 mmol) in N,N-dimethylformamide (20 mL) at 0° C. was added piperidine (8.0 mL, 80 mmol) and the mixture was warmed to room temperature then stirred 16 h. The reaction mixture was diluted with ethyl acetate (200 mL) and washed with a solution of brine and 2.0M aqueous sodium hydroxide (4:1 v/v). The organic phase was then dried over anhydrous sodium sulfate, filtered and concentrated to give ethyl 4-piperidin-1-ylbutanoate (6.8 g, 81% yield) as brown oil. MS (EI) for C11H21NO2: 200 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08648066B2
Source datasetuspto-grants-2014_02
ORD IDord-ae4805885de942df8959605d04797bae
Source noteuspto-grants-2014_02