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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1911317Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1911317

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
PatentnummerUS08604022B2
Quelldatensatzuspto-grants-2013_12
ORD IDord-79e16d86aada4d1a8cc4d74715806896
Quellennotizuspto-grants-2013_12