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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 735Erstellt: 25. Oktober 2026

tert-Butyl piperazine-1-carboxylate → Methyl 4-(4-Boc-1-piperazinyl)-2-chlorobenzoate

https://huagongshe.com/reaction/735

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukttert-Butyl piperazine-1-carboxylateHCID 143452—
EduktMethyl 4-Bromo-2-chlorobenzoateHCID 22058730—
ReagenzCesium carbonateHCID 10796—
KatalysatorBinap, (A+-)-HCID 634876—
KatalysatorPalladium (II) acetateHCID 4144353—
LösungsmittelTolueneHCID 1140—
ProduktMethyl 4-(4-Boc-1-piperazinyl)-2-chlorobenzoateHCID 7355396590,88%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

To a solution of palladium acetate (18.00 mg, 0.08 mmol) in dry toluene (16 mL) under nitrogen was added BINAP (100 mg, 0.16 mmol). The reaction was heated to 80 °C and stirred for 10 min. To the reaction was then added tert- butyl piperazine-1-carboxylate (299 mg, 1.60 mmol), cesium carbonate (261 mg, 0.80 mmol), potassium carbonate (222 mg, 1.60 mmol), 18-crown-6 (42.4 mg, 0.16 mmol) and methyl 4-bromo-2-chlorobenzoate (400 mg, 1.60 mmol). The reaction was stirred at 80°C overnight, filtered through celite and washed with small amounts of DCM. The filtrate was concentrated under reduced pressure and purified by flash chromatography on silica gel, eluting with mixtures of EtOAc and heptane, to afford tert-butyl 4-(3-chloro-4-(methoxycarbonyl)phenyl)piperazine-1-carboxylate (517 mg, 91 %) as a solid.

Herkunft & Nachweise

Quelldatensatz750 AstraZeneca ELN dataset
ORD IDord-879a784e2da64b7f993840feec5d14ac
Quellennotiz750 AstraZeneca ELN dataset