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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1483221Generated: October 31, 2026

Piperidine → 1-(But-3-yn-1-yl)piperidine

https://huagongshe.com/reaction/1483221

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromobut-1-yneHCID 11073464—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product1-(But-3-yn-1-yl)piperidineHCID 1315598640.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of piperidine (T1, 2.90 g, 34.0 mmol), potassium carbonate (3.00 g, 21.7 mmol), and 4-bromobut-1-yne (5.00 g, 37.6 mmol) in anhydrous acetonitrile (60 mL) was heated to 80° C. under nitrogen for 20 h. After this time, the reaction mixture was cooled to room temperature and diluted with water (50 mL). The resulting mixture was extracted with ethyl acetate (3×50 mL). The combined extracts were dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to afford compound T2 as light brown oil (1.89 g, 40%): MS (M+H) 138.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09416141B2
Source datasetuspto-grants-2016_08
ORD IDord-44db4023ee7d40b187ef8c09aec1667f
Source noteuspto-grants-2016_08