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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 35713Erstellt: 23. Oktober 2026

Triethylamine → N-t-butoxycarbonyl-L-alanyl-D-alanine benzyl ester

https://huagongshe.com/de/reaction/35713

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktDicyclohexylcarbodiimideHCID 10868—
EduktTert-butoxycarbonylalanineHCID 85082—
EduktD-Alanine, phenylmethyl ester, 4-methylbenzenesulfonate (1:1)HCID 2802425—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-t-butoxycarbonyl-L-alanyl-D-alanine benzyl esterHCID 13369188—

Reaktionsschritte

To a solution of 23.0 g. (0.121 m) of N-t-butoxycarbonyl-L-alanine, 42.6 g. (0.121 m) of D-alanine benzyl ester p-toluenesulfonic acid salt and 17 ml. (0.121 m) of triethylamine in 400 ml. of cold (0° C.) methylene chloride was added dropwise 25.0 g. (0.121 m) of dicyclohexylcarbodiimide in 100 ml. of methylene chloride. After stirring overnight at room temperature the solids were filtered and the filtrate concentrated to an oil. The residue was dissolved in 400 ml. of ethyl acetate which was washed with a 1% hydrochloric acid solution, a 10% potassium carbonate solution, water and a brine solution. The organic phase was separated, dried over magnesium sulfate and concentrated to an oil. The residue was triturated with diethyl ether and the resulting solids filtered under nitrogen, 16.0 g. An additional 12.7 g. of the desired product crystallized from the filtrate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04767743
Quelldatensatzuspto-grants-1988_08
ORD IDord-8a2f92c2d143402187baa2f3871614ad
Quellennotizuspto-grants-1988_08