Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1928545Erstellt: 24. Oktober 2026

Water → 4-[2-(2-Fluorophenoxy)ethyl]piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/de/reaction/1928545

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktCesium carbonateHCID 10796—
Edukttert-Butyl piperazine-1-carboxylateHCID 143452—
Edukt1-(2-Bromoethoxy)-2-fluorobenzeneHCID 2386106—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-[2-(2-Fluorophenoxy)ethyl]piperazine-1-carboxylic acid tert-butyl esterHCID 67298803—

Reaktionsschritte

To a solution of piperazine-1-carboxylic acid tert-butyl ester (2.79 g, 15 mmol) and 1-(2-bromoethoxy)-2-fluoro-benzene (3.28 g, 15 mmol) in DMF (6 mL) was added cesium carbonate (Cs2CO3, 9.75 g, 30 mmol). The mixture was stirred at room temperature for a day and then treated with water. The aqueous solution was extracted with ethyl acetate and the extract was washed with water and brine. The organic layer was concentrated and the residue was dried under the vacuum to yield the title compound quantitatively as an oil (5.1 g). 1H NMR (400 MHz, DMSO-d6): δ 1.39 (s, 9H), 2.44 (t, 4H), 2.73 (t, 2H), 3.29 (t, 4H), 4.45 (t, 2H), 6.93 (m, 1H), 7.11 (t, 1H), 7.18 (m, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08183374B2
Quelldatensatzuspto-grants-2012_05
ORD IDord-7d878bb266584c8b8fb8c18cda8af50d
Quellennotizuspto-grants-2012_05