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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1025426Erstellt: 26. Oktober 2026

Dimethylformamide → 2-(Trimethylsilyl)ethyl 3-[cyclopropyl(4-ethoxy-4-oxobutyl)sulfamoyl]benzoate

https://huagongshe.com/reaction/1025426

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktPotassium CarbonateHCID 11430—
EduktEthyl 4-bromobutyrateHCID 76300—
Edukt2-(Trimethylsilyl)ethyl 3-(cyclopropylsulfamoyl)benzoateHCID 71238446—
LösungsmittelWaterHCID 962—
Produkt2-(Trimethylsilyl)ethyl 3-[cyclopropyl(4-ethoxy-4-oxobutyl)sulfamoyl]benzoateHCID 7123873787,7%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A mixture of 2.12 g of 2-(trimethylsilyl)ethyl 3-(cyclopropylsulfamoyl)benzoate, 1.45 g of ethyl 4-bromobutyrate, 2.57 g of potassium carbonate, and 21 mL of DMF was stirred at 80° C. overnight. To the reaction mixture was added water, followed by extraction with ethyl acetate. The organic layer was washed with water and saturated brine in this order, then dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane-ethyl acetate) to obtain 2.48 g of 2-(trimethylsilyl)ethyl 3-[cyclopropyl(4-ethoxy-4-oxobutyl)sulfamoyl]benzoate as a colorless oily substance. ESI+: 456

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08729068B2
Quelldatensatzuspto-grants-2014_05
ORD IDord-6bf468a48dd04aa49424f7648e7f56cd
Quellennotizuspto-grants-2014_05