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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1985625Generated: November 2, 2026

Propargyl bromide → tert-Butyl 4-(prop-2-yn-1-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1985625

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantSodium CarbonateHCID 10340—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
SolventAcetonitrileHCID 6342—
Producttert-Butyl 4-(prop-2-yn-1-yl)piperazine-1-carboxylateHCID 1128753874.6%

Reaction Conditions

Temperature50 °C

Reaction Steps

To the degassed solution of piperazine-1-carboxylic acid tert-butyl ester (0.5 g, 2.69 mmol) in acetonitrile (5 mL) was added Na2CO3 (0.854 g, 8.05 mmol) and mixture was stirred for 20 min. The suspension was heated to 50° C. and 3-bromo-propyne (448.65 μl, 4.03 mmol) was added. The solvent was evaporated and the residue was extracted with EtOAc and water. Organic layer was washed with NaCl and NaHCO3 (2×20 ml), dried over K2CO3 and evaporated in vacuum yielding 0.45 g of the title product as yellowish oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07547679B2
Source datasetuspto-grants-2009_06
ORD IDord-005433dca4ca466db46700003881c46c
Source noteuspto-grants-2009_06