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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 16821Erstellt: 24. Oktober 2026

Acetic Acid → tert-Butyl 4-cyclopropylpiperazine-1-carboxylate

https://huagongshe.com/de/reaction/16821

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
Edukttert-Butyl piperazine-1-carboxylateHCID 143452—
Edukt(1-Ethoxycyclopropoxy)trimethylsilaneHCID 2734686—
EduktSodium cyanoborohydrideHCID 5003444—
LösungsmittelMethanolHCID 887—
LösungsmittelTetrahydrofuranHCID 8028—
Produkttert-Butyl 4-cyclopropylpiperazine-1-carboxylateHCID 2029452468,3%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

A solution of tert-butyl piperazine-1-carboxylate (9.31 g, 50 mmol), [(1-ethoxycyclopropyl)oxy]trimethylsilane (20.11 mL, 100.00 mmol) and acetic acid(14.31 mL, 250.00 mmol) in tetrahydrofuran (100 mL), methanol (10 mL) was treated with sodium cyanoborohydride (4.71 g, 75.00 mmol) at 20° C. The resulting solution was stirred at 60° C. for 18 h. The reaction mixture was cooled, filtered and evaporated to dryness. 1N HCl (40 ml) and water (60 ml) were added and the solution extracted with ethyl acetate (3×50 ml). The aqueous layer was basified to pH 10 with solid potassium carbonate and extracted with ethyl acetate (4×50 ml). The organic extracts were washed with saturated sodium chloride solution (50 ml) and dried over MgSO4, filtered and evaporated to dryness to give tert-butyl 4-cyclopropylpiperazine-1-carboxylate (7.73 g, 68.3%) as a white waxy solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07737149B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-96114825bb9d43c79c23579a8e9e0a18
Quellennotizuspto-grants-2010_06