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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 16745Erstellt: 24. Oktober 2026

5-Bromothiophene-2-carbaldehyde → Tert-butyl 4-(5-formylthiophen-2-yl)piperazine-1-carboxylate

https://huagongshe.com/de/reaction/16745

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-Bromothiophene-2-carbaldehydeHCID 78428—
EduktDiisopropylethylamineHCID 81531—
Edukttert-Butyl piperazine-1-carboxylateHCID 143452—
LösungsmittelDimethyl SulfoxideHCID 679—
ProduktTert-butyl 4-(5-formylthiophen-2-yl)piperazine-1-carboxylateHCID 2806529873%

Reaktionsbedingungen

Temperatur130 °C

Reaktionsschritte

A mixture of 5-bromothiophene-2-carboxaldehyde (3.82 g, 20.0 mmol), tert-butyl piperazine-1-carboxylate (4.1 g, 22.0 mmol), N-ethyl-N,N-diisopropylamine (7.0 ml, 40.0 mmol) and dimethylsulphoxide (5.0 ml) were stirred at 130° C. under an atmosphere of nitrogen for 18 h. The cooled mixture was partitioned between ethyl acetate and water. The organics were washed with water, brine, dried over magnesium sulphate and evaporated. The resultant dark red solid was purified by silica column chromatography, eluting with dichloromethane followed by ethyl acetate/dichloromethane (15%) to give tert-butyl 4-(5-formylthien-2-yl)piperazine-1-carboxylate (4.3 g, 73%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07737149B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-c417a6ea2d5f4f54842f9fa9a25eed89
Quellennotizuspto-grants-2010_06