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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 32705Erstellt: 23. Oktober 2026

Cesium carbonate → Tert-butyl 4-[4-(trifluoromethoxy)phenyl]piperazine-1-carboxylate

https://huagongshe.com/de/reaction/32705

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCesium carbonateHCID 10796—
Edukttert-Butyl piperazine-1-carboxylateHCID 143452—
Edukt1-Bromo-4-(trifluoromethoxy)benzeneHCID 521008—
EduktBinap, (A+-)-HCID 634876—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelTolueneHCID 1140—
LösungsmittelEthyl AcetateHCID 8857—
ProduktTert-butyl 4-[4-(trifluoromethoxy)phenyl]piperazine-1-carboxylateHCID 5979353713%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a mixture of cesium carbonate (1.88 g, 5.7 mmol), palladium(II)acetate (46.1 mg, 0.205 mmol), rac-2,2′-Bis(diphenylphosphino)-1,1′-binaphthyl (192 mg, 0.31 mmol), tert-Butyl-1-piperazine carboxylate (928 mg, 4.93 mmol) and 1-Bromo-4-(trifluoromethoxy)benzene (1 g, 4.11 mmol) was added degazed toluene (10 ml). The mixture was heated to 100° C. for 4 hours. The mixture was cool to room temperature, diluted with ethylacetate, filtered and the solvent was removed in vacuo. The crude oil was chromatographed over silica gel: eluent: heptane/ethylacetate 0-10% over 20 minutes to provide the title compound (180 mg, 13%) as a yellow solid, MS (m/e): 347.4 (M+H, 100%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07427612B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-b45b3fee9e4a4e5f8550d6537c6cfb9b
Quellennotizuspto-grants-2008_09