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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2214220Generated: November 1, 2026

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

https://huagongshe.com/reaction/2214220

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 CH2Cl2 (50 ml) 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 water bath at 60° C. without vacuum. Once most solvent had been evaporated off, dried the clear oil under high vacuum at RT for 30 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105682B2
Source datasetuspto-grants-2006_09
ORD IDord-9562010fe65444b0bea2481bd49ac41a
Source noteuspto-grants-2006_09