Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 557Erstellt: 23. Oktober 2026

p-Bromoacetophenone → Tert-butyl 4-(4-acetylphenyl)piperazine-1-carboxylate

https://huagongshe.com/de/reaction/557

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp-BromoacetophenoneHCID 7466—
Edukttert-Butyl piperazine-1-carboxylateHCID 143452—
ReagenzCesium carbonateHCID 10796—
KatalysatorBinap, (A+-)-HCID 634876—
KatalysatorPalladium (II) acetateHCID 4144353—
LösungsmittelTolueneHCID 1140—
ProduktTert-butyl 4-(4-acetylphenyl)piperazine-1-carboxylateHCID 2113619052,48%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

In a CEM MW vial, p-Bromoacetophenone (729 ml, 6.03 mmol),tert-Butyl 1-piperazinecarboxylate (1.684 g, 9.04 mmol),racemic-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl (0.375 g, 0.60 mmol),Palladium (II) acetate (0.135 g, 0.60 mmol),Cesium carbonate (3.93 g, 12.06 mmol) was taken in toluene (10 ml).The RM was subjected to MW power of 300W,temp 120°C for 45 minutes. The LCMS was checked showed the formation of required mass. Work-up: The RM was passed through hyflow bed and filtrate was evaporated and chrmatographed using Ethyl acetate hexane to obtain tert-butyl 4-(4-acetylphenyl)piperazine-1-carboxylate (0.963 g, 52.5 %).

Herkunft & Nachweise

Quelldatensatz750 AstraZeneca ELN dataset
ORD IDord-c7d1825ed35e4dffbc57a0b9b8fa9354
Quellennotiz750 AstraZeneca ELN dataset