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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467588Generated: October 30, 2026

Piperazine → HCID 68721387, compound

https://huagongshe.com/reaction/467588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant1-Bromo-2-ChloroethaneHCID 7849—
ReactantPotassium CarbonateHCID 11430—
SolventAcetonitrileHCID 6342—
ProductHCID 68721387HCID 6872138761%

Reaction Conditions

Temperature25 °C

Reaction Steps

The piperazine Example 2 (500 mg, 1.36 mmol), BrCH2CH2Cl (0.7 mL), and K2CO3 (320 mg, 2.3 mmol) were taken up in CH3CN (2 mL) and stirred at 25° C. for 18 h. The solution was partitioned between EtOAc and water. The aqueous layer was extracted with EtOAc. The combined organic layers were washed with brine and dried (MgSO4), Filtration and concentration gave a yellow oil. The residue was purified via gradient flash chromatography (0-15% EtOAc in CH2Cl2, SiO2) which gave 357 mg (61%) of the chloro-ethyl piperazine as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08623873B2
Source datasetuspto-grants-2014_01
ORD IDord-071b424bb842443aa56172a1a890d067
Source noteuspto-grants-2014_01