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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 352776Erstellt: 24. Oktober 2026

Benzyl Bromide → Tert-butyl 4-benzylpiperazine-1-carboxylate

https://huagongshe.com/de/reaction/352776

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl BromideHCID 7498—
EduktTriethylamineHCID 8471—
Edukttert-Butyl piperazine-1-carboxylateHCID 143452—
LösungsmittelAcetonitrileHCID 6342—
ProduktTert-butyl 4-benzylpiperazine-1-carboxylateHCID 584330—

Reaktionsschritte

In acetonitrile (80 ml), tert-butyl 1-piperazine carboxylate (2.50 g) was dissolved. Under ice cooling, benzyl bromide (1.59 ml) and triethylamine (1.87 ml) were added dropwise to the resulting solution, followed by stirring at room temperature for 90 minutes. After the solvent was distilled off under reduced pressure, distilled water and dichloromethane were added to the residue to separate the organic layer. The organic layer was washed with saturated aqueous NaCl solution and dried over anhydrous sodium sulfate. The residue obtained by distilling off the solvent under reduced pressure was purified by chromatography on a silica gel column (ethyl acetate:hexane=1:20 to 1:5), whereby the title compound (3.12 g, 84%) was obtained as colorless powder.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06747023B1
Quelldatensatzuspto-grants-2004_06
ORD IDord-db6b2e86d50d483baa4043eb53a4adb0
Quellennotizuspto-grants-2004_06