Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1433748Erstellt: 25. Oktober 2026

Trifluoroacetic acid → (2S,3S)-2-amino-N-(4-bromo-2-chloro-phenyl)-3-phenyl-butyramide

https://huagongshe.com/reaction/1433748

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrifluoroacetic acidHCID 6422—
EduktChlorine monoxideHCID 24646—
Edukt4-Bromo-2-chloroanilineHCID 610169—
Edukt(2S,3S)-2-((tert-Butoxycarbonyl)amino)-3-phenylbutanoic acidHCID 7021178—
LösungsmittelPyridineHCID 1049—
Produkt(2S,3S)-2-amino-N-(4-bromo-2-chloro-phenyl)-3-phenyl-butyramideHCID 6900970355,9%

Reaktionsbedingungen

Temperatur-20 °C

Reaktionsschritte

4-Bromo-2-chloro-aniline (325 mg, 1.58 mmol) and (S,S)-2-tert-butoxycarbonylamino-3-phenyl-butyric acid (440 mg, 1.58 mmol) in pyridine (5 mL) were cooled to −30° C. Phosporus oxychloride (0.158 mL, 1.7 mmol) was added and stirred at −20° C. for 2 hours. The mixture was poured into ice water and extracted with ethyl acetate (3×). The combined organic extracts were washed with water, brine, dried over sodium sulfate and concentrated in vacuo. The residue was dissolved in dichloromethane (5 mL) at 0° C. and trifluoroacetic acid (3 mol) added. Stirring was continued for 2 hours at 0° C. The mixture was evaporated and the residue dissolved in ether. The ether solution was basified with saturated aqueous sodium bicarbonate and extracted with ether. The organic extracts were washed with brine, dried over sodium sulfate and evaporated to give (2S,3S)-2-amino-N-(4-bromo-2-chloro-phenyl)-3-phenyl-butyramide (325 mg, 55%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07612212B2
Quelldatensatzuspto-grants-2009_11
ORD IDord-0c55c916f03d40cbb741710fd867c04b
Quellennotizuspto-grants-2009_11