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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 16783Erstellt: 24. Oktober 2026

Acetic Acid → Tert-butyl 4-cyclobutylpiperazine-1-carboxylate

https://huagongshe.com/de/reaction/16783

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktCyclobutanoneHCID 14496—
Edukttert-Butyl piperazine-1-carboxylateHCID 143452—
EduktSodium cyanoborohydrideHCID 5003444—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktTert-butyl 4-cyclobutylpiperazine-1-carboxylateHCID 5742395153,5%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

Water (0.3 mL), cyclobutanone (2.000 g, 28.53 mmol) and acetic acid (3.48 mL, 60.86 mmol) were added to a stirred solution of tert-butyl piperazine-1-carboxylate (3.54 g, 19.02 mmol) in THF (40 mL) under nitrogen. Sodium cyanoborohydride (1.793 g, 28.53 mmol) was added portionwise over a period of 10 mins. The resulting mixture was stirred at 60° C. for 19 h. The reaction mixture was evaporated to dryness and mixed with water (80 mL) and 1M HCl (25 mL). The solution was washed with EtOAc (2×50 mL), basified with K2CO3 and extracted with EtOAc (2×30 mL). The organic layer was washed with saturated brine and dried over MgSO4, filtered and evaporated to afford pure tert-butyl 4-cyclobutylpiperazine-1-carboxylate (2.445 g, 53.5%) as a colourless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07737149B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-d9ddea175d7547909e7151d1e5cfebeb
Quellennotizuspto-grants-2010_06