HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749941Generated: October 30, 2026
Water → tert-Butyl 4-(prop-2-yn-1-yl)piperazine-1-carboxylate
https://huagongshe.com/reaction/1749941
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Propargyl bromide | HCID 7842 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | tert-Butyl 4-(prop-2-yn-1-yl)piperazine-1-carboxylate | HCID 11287538 | 83.9% |
Reaction Steps
A solution of propargyl bromide (0.766 g, 6.44 mmol) in acetonitrile (25 mL) was added with 1-tert-butoxycarbonylpiperazine (1.00 g, 5.37 mmol) and potassium carbonate (1.11 g, 8.03 mmol), and the mixture was stirred at 60° C. for 4 hours. The reaction mixture was added with water, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, then dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane/ethyl acetate) to obtain tert-butyl 4-(prop-2-ynyl)piperazine-1-carboxylate (1.01 g, 83%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09156827B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-1bcd7fb0f58d443e8f480066e71fe3ee |
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| Source note | uspto-grants-2015_10 |
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