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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1023211Erstellt: 26. Oktober 2026

Water → Tert-butyl 4-(benzo[d][1,3]dioxol-4-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1023211

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktCesium carbonateHCID 10796—
Edukttert-Butyl piperazine-1-carboxylateHCID 143452—
Edukt4-Bromo-1,3-benzodioxoleHCID 2776189—
Katalysatorpalladium(II) acetateHCID 167845—
KatalysatorBinap, (A+-)-HCID 634876—
LösungsmittelTolueneHCID 1140—
ProduktTert-butyl 4-(benzo[d][1,3]dioxol-4-yl)piperazine-1-carboxylateHCID 6828275875,5%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

Tert-butyl piperazine-1-carboxylate (1.11 g, 5.97 mmol) was added to a solution of 4-bromobenzo[d][1,3]dioxole (1 g, 4.97 mmol) in Toluene (15.0 ml). The resulting suspension was degassed using a stream of argon. Cesium carbonate (2.27 g, 558 μl, 6.96 mmol), racemic-2,2′-bis(diphenylphosphino)-1,1′-binaphtyl (232 mg, 373 μmol, Eq: 0.075) and Palladium (II) Acetate (55.8 mg, 249 μmol) were added to this mixture. The reaction was then heated at 100° C. over night. The reaction was cooled to rt, 40 ml of water was added and the mixture was extracted with Ethyl Acetate (2×80 ml). The organic layers were dried over MgSO4 and concentrated under vacuum. The crude material was purified by flash chromatography (silica gel, 50 g, 0% to 50% EtOAc in heptane). to yield tert-butyl 4-(benzo[d][1,3]dioxol-4-yl)piperazine-1-carboxylate as a white solid (1.15 g, 75%). MS (ISP) m/z=307.4 [(M+H)+].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08722683B2
Quelldatensatzuspto-grants-2014_05
ORD IDord-1b75482718694e318c46573820c0ba65
Quellennotizuspto-grants-2014_05