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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2190256Erstellt: 24. Oktober 2026

tert-Butyl piperazine-1-carboxylate → tert-Butyl 4-((3-bromofuran-2-yl)methyl)piperazine-1-carboxylate

https://huagongshe.com/de/reaction/2190256

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukttert-Butyl piperazine-1-carboxylateHCID 143452—
Edukt3-Bromo-2-furaldehydeHCID 3367271—
EduktSodium triacetoxyborohydrideHCID 5049666—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelEthyl AcetateHCID 8857—
Produkttert-Butyl 4-((3-bromofuran-2-yl)methyl)piperazine-1-carboxylateHCID 7107912892,5%

Reaktionsschritte

To a solution of 3-bromofuran-2-carbaldehyde (500 mg, 2.85 mmol) and tert-butyl piperazine-1-carboxylate (1.1 g, 5.71 mmol) in CH2Cl2 (10 mL) was added sodium triacetoxyborohydride (1.2 g, 5.71 mmol). The mixture was stirred at room temperature for 12 hours. The reaction mixture was diluted with EtOAc (100 mL). The organic phase was washed with aqueous NaHCO3 and brine then dried (MgSO4), filtered and concentrated to dryness. The residue was purified by column chromatography (silica, 0-10% MeOH in CH2Cl2) to afford the sub-title compound (910 mg, 92%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08324264B1
Quelldatensatzuspto-grants-2012_12
ORD IDord-21fe05743de049d4a49b049ec970359d
Quellennotizuspto-grants-2012_12