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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 46001Erstellt: 23. Oktober 2026

4-Bromopyridine → tert-Butyl 4-(pyridin-4-yl)piperazine-1-carboxylate

https://huagongshe.com/de/reaction/46001

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-BromopyridineHCID 14268—
Edukttert-Butyl piperazine-1-carboxylateHCID 143452—
EduktBinap, (A+-)-HCID 634876—
EduktSodium t-butoxideHCID 23676156—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelSodium chloride; waterHCID 57417360—
Produkttert-Butyl 4-(pyridin-4-yl)piperazine-1-carboxylateHCID 5743681847%

Reaktionsschritte

To a degassed solution of 4-bromopyridine (1 equiv.), tert-butyl piperazine-1-carboxylate (16 mmol, 1.2 equiv.) and NaOtBu (3.4 equiv.) in toluene were added Pd(OAc)2 (2 mol %) and BINAP (1 mol %) and the resulting solution was refluxed for 3 h. The reaction mixture was cooled, diluted with ethyl acetate and given water and brine washes respectively. The organic layer was dried over sodium sulfate, the solvent removed in vacuo and the crude product purified by column chromatography (silica). Yield: 47%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08541573B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-1fb23cebb0544832ac7e9595990b2180
Quellennotizuspto-grants-2013_09