Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 11254Erstellt: 25. Oktober 2026

Chlorotrimethylsilane → 2-Butyrylaminobutyric acid

https://huagongshe.com/reaction/11254

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChlorotrimethylsilaneHCID 6397—
EduktAlpha-Aminobutyric AcidHCID 6657—
EduktTriethylamineHCID 8471—
EduktButyryl chlorideHCID 8855—
EduktSodium HydroxideHCID 14798—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-Butyrylaminobutyric acidHCID 12408866—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

25.78 g of 2-aminobutyric acid (250 mmol) and 55.66 g (550 mmol) of triethylamine are dissolved in 250 ml of dichloromethane, and the solution is cooled to 0° C. 59.75 g (550 mmol) of trimethylsilyl chloride are added dropwise, and the solution is stirred at room temperature for 1 hour and at 40° C. for one hour. After cooling to −10° C., 26.64 g (250 mmol) of butyryl chloride are added dropwise, and the resulting mixture is stirred at −10° C. for 2 hours and at room temperature for one hour. With ice-cooling, 125 ml of water are added dropwise, and the reaction mixture is stirred at room temperature for 15 minutes. Aqueous sodium hydroxide solution is added to the organic phase, and the organic solvent is removed under reduced pressure. The residue is acidified and the precipitated solid is triturated once with water and twice with petroleum ether and dried under reduced pressure at 45° C. 29.1 g (67%) of a colorless solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07098207B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-46b5a06419784ab4aa0ab701d258a09a
Quellennotizuspto-grants-2006_08