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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 654971Erstellt: 23. Oktober 2026

Dichloromethane → glycyl-D-alanine benzyl ester hydrochloride

https://huagongshe.com/de/reaction/654971

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
EduktTriethylamineHCID 8471—
EduktDicyclohexylcarbodiimideHCID 10868—
EduktD-Alanine, phenylmethyl ester, 4-methylbenzenesulfonate (1:1)HCID 2802425—
EduktN-t-butyloxy-carbonylglycineHCID 86746012—
Produktglycyl-D-alanine benzyl ester hydrochlorideHCID 6778873070%

Reaktionsschritte

To a cold (0° C.) solution of 100 ml. methylene chloride containing 10 g. (57 mmol) of N-t-butyloxy-carbonylglycine, 20 g. (57 mmol) of D-alanine benzyl ester p-toluene sulfonic acid salt and 5.77 g. (57 mmol) of triethylamine was added 12.3 g. (60 mmol) of dicyclohexylcarbodiimide and the resulting reaction mixture allowed to warm to room temperature. After 18 hours the mixture was filtered and the filtrate concentrated in vacuo. The residue was dissolved in 200 ml. of ethyl acetate and the organic layer washed with 2.5% hydrochloric acid, water, a saturated sodium bicarbonate solution and a brine solution. The organic layer was separated, dried over magnesium sulfate and evaporated under reduced pressure. To the resulting oil 200 ml. of dioxane saturated with hydrogen chloride was added. After 30 minutes 400 ml. of diethyl ether was added and the product filtered under nitrogen, 10.9 g. (70% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05134225
Quelldatensatzuspto-grants-1992_07
ORD IDord-887fbe5d39264107a14807013c138ef8
Quellennotizuspto-grants-1992_07