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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1619368Generated: November 1, 2026

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

https://huagongshe.com/reaction/1619368

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 1315598643.1%

Reaction Steps

A solution of piperidine (2.9 g, 33.8 mmol), 4-bromobut-1-yne (5 g, 37.6 mmol) and K2CO3 (3 g, 2.2 mmol) in CH3CN was stirred at 80° C. for 2 h. After it was cooled to room temperature, the solution was diluted with H2O and extracted with ethyl acetate (3×200 mL). Then the combined organic layers were dried over Na2SO4 and concentrated to give 2 g of the crude product, which was directly used for the next step without further purification. MS (ESI): 138 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772301B2
Source datasetuspto-grants-2014_07
ORD IDord-f9b7ea33b07a4db1a31e45147d9b6071
Source noteuspto-grants-2014_07