HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 708325Generated: October 30, 2026
Potassium Carbonate → Tert-butyl 4-(but-3-yn-1-yl)piperazine-1-carboxylate
https://huagongshe.com/reaction/708325
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | 4-Bromobut-1-yne | HCID 11073464 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Tert-butyl 4-(but-3-yn-1-yl)piperazine-1-carboxylate | HCID 72213388 | 86.1% |
Reaction Steps
To a solution of 1-Boc-piperazine (0.5 g, 2.68 mmol) in acetonitrile (2.5 mL) was added K2CO3 (0.55 g, 4.02 mmol) followed by 4-bromo-1-butyne (0.39 g, 2.95 mmol). The mixture was heated at 60° C. for 6 h, allowed to come to room temperature, diluted with water and extracted with EtOAc (2×15 mL). The combined organic layers washed with water, brine, dried over Na2SO4 and concentrated under vacuo to afford the title compound (0.55 g, 86%); LCMS: m/z=239.10 (M+1). Method 2minLowp.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09174978B2 |
|---|
| Source dataset | uspto-grants-2015_11 |
|---|
| ORD ID | ord-73850401e58f425daf9602b359bfec31 |
|---|
| Source note | uspto-grants-2015_11 |
|---|