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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1586443Generated: November 1, 2026

Piperazine → 1-Butylpiperazine

https://huagongshe.com/reaction/1586443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantButyl bromideHCID 8002—
ReactantSodium HydroxideHCID 14798—
SolventEthanolHCID 702—
Product1-ButylpiperazineHCID 42432229.2%

Reaction Steps

Anhydrous piperazine (19.5 g) was dissolved in ethanol (100 ml), and a solution of 1-bromobutane (24.8 g) in ethanol (50 ml) was added dropwise over a period of 20 minutes at room temperature. After stirring overnight, the reaction solution was filtered off with Celite, and the solvent was distilled off under reduced pressure. To the residue obtained was added a 40% aqueous solution of sodium hydroxide, and extracted with ether three times. The ether layer was dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (methylene chloride:methanol:aqueous ammonia=90:10:0.5) to give the title compound (7.53 g) as a yellow oily substance. Yield=29%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05945434
Source datasetuspto-grants-1999_08
ORD IDord-ce09ba1a1cb34bdeae8b1aa6ed715b94
Source noteuspto-grants-1999_08