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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 557372Generated: October 29, 2026

Piperidine → 1-(piperidin-1-yl)prop-2-en-1-one

https://huagongshe.com/reaction/557372

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantAcryloyl chlorideHCID 13140—
SolventDichloromethaneHCID 6344—
Product1-(piperidin-1-yl)prop-2-en-1-oneHCID 350473—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 0° C. solution of acryloyl chloride (4.576 g, 50.558 mmol) in 50 ml of CH2Cl2 was added dropwise and very carefully piperidine (4.305 g, 50.558 mmol). The reaction flask was vented during the exothermic addition. After the addition was completed, the white slurry was stirred at 0° C. for 40 min and at RT for 1 h. The reaction was diluted with 70 ml CH2Cl2 and washed first with about 60 ml 2N HCl and then with about 60 ml of a mix of 2N NaOH and brine. The organic layer was dried over Na2SO4. The solution was evaporated by heating in a H2O bath at 60° C. without vacuum. Once most solvent had been evaporated off, it was furthered dried to a clear oil under high vacuum at RT for 30 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08058445B2
Source datasetuspto-grants-2011_11
ORD IDord-11ed25a29ee7437a8423d0f7ff9e26f8
Source noteuspto-grants-2011_11