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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 16782Erstellt: 25. Oktober 2026

Trifluoroacetic acid → 1-Cyclobutylpiperazine

https://huagongshe.com/reaction/16782

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrifluoroacetic acidHCID 6422—
EduktTert-butyl 4-cyclobutylpiperazine-1-carboxylateHCID 57423951—
LösungsmittelDichloromethaneHCID 6344—
Produkt1-CyclobutylpiperazineHCID 473860230,2%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Trifluoroacetic acid (7.84 mL, 101.73 mmol) was added to a stirred solution of tert-butyl 4-cyclobutylpiperazine-1-carboxylate (2.445 g, 10.17 mmol) in DCM (25 mL) cooled to 0° C. under nitrogen and stirred at 20° C. for 24 h. The reaction mixture was evaporated to dryness and diluted with DCM (30 mL). This was then washed with saturated NaHCO3 (2×10 mL) and the organic layers evaporated to dryness. Product was still present in the aqueous layer, so this was basified with 2M NaOH and extracted with DCM (3×10 mL) and EtOAc (1×10 mL). Organic fractions were combined and evaporated to dryness to afford 1-cyclobutylpiperazine (0.430 g, 30.1%). 1H NMR (399.9 MHz, DMSO-d6) δ 1.60-1.67 (2H, m), 1.72-1.80 (2H, m), 1.93-1.97 (2H, m), 2.25 (4H, s), 2.57-2.60 (1H, d), 2.82 (4H, t)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07737149B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-7fc4e6f9d29d4002956b76118a511d42
Quellennotizuspto-grants-2010_06