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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 13558Erstellt: 25. Oktober 2026

Sodium Hydroxide → tert-Butyl 4-cyclopropylpiperazine-1-carboxylate

https://huagongshe.com/reaction/13558

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium HydroxideHCID 14798—
Edukttert-Butyl piperazine-1-carboxylateHCID 143452—
Edukt(1-Ethoxycyclopropoxy)trimethylsilaneHCID 2734686—
EduktSodium cyanoborohydrideHCID 5003444—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkttert-Butyl 4-cyclopropylpiperazine-1-carboxylateHCID 20294524—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

A mixture of tert-butyl piperazine-1-carboxylate (75.0 g), THF (500 mL), methanol (500 mL), [(1-ethoxycyclopropyl)oxy]trimethylsilane (161 mL), NaBH3CN (38.0 g), and acetic acid (37 mL) was heated at 60° C. for 5 h. The mixture was cooled to room temperature, treated with water (30 mL) and stirred for 5 min. The mixture was then treated with 1 N NaOH (130 mL) and was further stirred for 15 min. The mixture was concentrated, and the remaining aqueous solution was extracted with CH2Cl2 (500 mL). The organic layer was washed with 1 N NaOH (500 mL). The combined aqueous layers were extracted with CH2Cl2 (150 mL). The combined organic layers were washed with brine (400 mL), dried (Na2SO4), and concentrated to yield the title compound as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07728129B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-db7dbad0b7b94f2588869652ef25d01f
Quellennotizuspto-grants-2010_06