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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1464221Erstellt: 25. Oktober 2026

Water → N-(Benzyloxycarbonyl)-L-aspartyl-L-phenylalanine methyl ester

https://huagongshe.com/reaction/1464221

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium AcetateHCID 517045—
Edukt(S)-Benzyl (tetrahydro-2,5-dioxo-3-furyl)carbamateHCID 11128682—
EduktL-phenylalanine methyl ester sulfateHCID 20841682—
LösungsmittelAcetic AcidHCID 176—
ProduktN-(Benzyloxycarbonyl)-L-aspartyl-L-phenylalanine methyl esterHCID 1015963073,1%

Reaktionsschritte

In 100.4 g of acetic acid, 25.1 g (0.1 mole) of N-benzyloxycarbonyl-L-aspartic anhydride was suspended and 22.7 g (0.1 mole) of L-phenylalanine methyl ester sulfate was added with stirring at 5°-10° C. Successively 17.6 g (0.21 mole) of sodium acetate was added at the same temperature. The reaction was carried out for 4 hours with stirring at the same temperature. Thereafter 87.1 g of water was added to the reaction mixture to adjust the concentration of organic carboxylic acid to 53.5% by weight. After cooling to 0°-5° C., precipitated crystals were filtered, washed and dried. Crystals of N-benzyloxycarbonyl-α-L-aspartyl-L-phenylalanine methyl ester were obtained. The yield was 31.2 g (73.1% yield on L-phenylalanine methyl ester sulfate).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05302743
Quelldatensatzuspto-grants-1994_04
ORD IDord-a893da5500e64c718ebcd50755c54d72
Quellennotizuspto-grants-1994_04