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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant4-Bromobut-1-yneHCID 11073464—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductTert-butyl 4-(but-3-yn-1-yl)piperazine-1-carboxylateHCID 7221338886.1%

Reaction Conditions

Temperature60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174978B2
Source datasetuspto-grants-2015_11
ORD IDord-73850401e58f425daf9602b359bfec31
Source noteuspto-grants-2015_11