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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 331117Erstellt: 25. Oktober 2026

Potassium Hydroxide → 4-[3-(4-Chloro-phenoxy)-benzyl]-piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/331117

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium HydroxideHCID 14797—
Edukttert-Butyl piperazine-1-carboxylateHCID 143452—
Edukt3-(4-Chlorophenoxy)benzaldehydeHCID 616015—
EduktSodium triacetoxyborohydrideHCID 5049666—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-[3-(4-Chloro-phenoxy)-benzyl]-piperazine-1-carboxylic acid tert-butyl esterHCID 6741354175%

Reaktionsschritte

A solution of piperazine-1-carboxylic acid tert-butyl ester (19.6 g, 105 mmol) and 3-(4-chloro-phenoxy)-benzaldehyde (24.4 g, 105 mmol) in THF (90 mL) was treated with NaB(OAc)3H (33.4 g, 158 mmol). After 3 h, the resulting mixture was treated with 10% aq. KOH (500 mL). The aqueous phase was extracted with EtOAc (2×500 mL) then saturated aqueous NaCl (200 mL). The organic extracts were combined, dried (MgSO4) and purified (FCC) to give 4-[3-(4-chloro-phenoxy)-benzyl]-piperazine-1-carboxylic acid tert-butyl ester (29.6 g, 75%). MS (ESI+): calcd for C22H27ClN2O3 m/z 402.17, found 403.2 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08877769B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-3263a016ae2a4704b1a099e6813fb1c3
Quellennotizuspto-grants-2014_11