HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238518Generated: October 29, 2026
Piperidine → 1-(piperidin-1-yl)prop-2-en-1-one
https://huagongshe.com/reaction/238518
Participants
| Role | Name | HCID | Charge |
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| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Acryloyl chloride | HCID 13140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(piperidin-1-yl)prop-2-en-1-one | HCID 350473 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08642624B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-454d7df1c2d84b2ebc5797e3a73f04be |
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| Source note | uspto-grants-2014_02 |
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