HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6791Generated: October 25, 2026
Propargyl bromide → 4-Methyl-1-(prop-2-yn-1-yl)piperidine
https://huagongshe.com/reaction/6791
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propargyl bromide | HCID 7842 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Methylpiperidine | HCID 69381 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-Methyl-1-(prop-2-yn-1-yl)piperidine | HCID 11355509 | 92% |
Reaction Steps
At 0–5° C., propargyl bromide (12.01 g) was added dropwise with stirring to a suspension of 4-methylpiperidine (10.0 g) and potassium carbonate (13.96 g) in dry acetone (80 ml). The mixture was stirred at 50° C. for 6 hours and then filtered. The filtrate was concentrated under reduced pressure and the residue was taken up in dichloromethane. The organic phase was washed with water (3×15 ml), dried with sodium sulfate and concentrated under reduced pressure. Distillation of the residue under reduced pressure gave 12.73 g of an oil of boiling point 60° C./16 mm Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07084158B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-3d1eef909b754b8da0b694cdccfec3a6 |
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| Source note | uspto-grants-2006_08 |
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