Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 127571Erstellt: 25. Oktober 2026

Triethylamine → N-(2-chloro-6-nitrobenzyl)-L-alanine ethyl ester

https://huagongshe.com/reaction/127571

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt2-(Bromomethyl)-1-chloro-3-nitrobenzeneHCID 91858—
EduktL-Alanine, ethyl ester, hydrochloride (1:1)HCID 2724356—
LösungsmittelEthanolHCID 702—
ProduktN-(2-chloro-6-nitrobenzyl)-L-alanine ethyl esterHCID 5370892591,7%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

18.24 g of L-alanine ethyl ester hydrochloride in 60 ml of ethanol was added dropwise to a mixture of 25 ml of triethylamine in 60 ml of ethanol and the mixture was heated to 80° C. The resulting solution was added dropwise at this temperature to a solution of 15 g of α-bromo-2-chloro-6-nitrotoluene in 60 ml of ethanol. The mixture was stirred at 80° C. overnight and then evaporated to dryness. The residue was treated with 150 ml of deionised water and extracted twice with 100 ml of methylene chloride. The methylene chloride extracts were washed with water, dried and evaporated. The resulting product was purified by chromatography on silica gel with methylene chloride/5% methanol. There were obtained 15.75 g (91% of theory) of N-(2-chloro-6-nitrobenzyl)-L-alanine ethyl ester; nD20 =1.5267.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04256748
Quelldatensatzuspto-grants-1981_03
ORD IDord-b36b9db07ec04c54a12306153c9f1ab9
Quellennotizuspto-grants-1981_03