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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 64783Erstellt: 23. Oktober 2026

Dl-Phenylalanine → L-phenylalanine N-carbobenzoxy-L-aspartic acid

https://huagongshe.com/de/reaction/64783

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDl-PhenylalanineHCID 994—
EduktSulfuric AcidHCID 1118—
EduktSodium HydroxideHCID 14798—
EduktD-PhenylalanineHCID 71567—
EduktN-(Benzyloxycarbonyl)aspartic acidHCID 2723942—
LösungsmittelWaterHCID 962—
ProduktL-phenylalanine N-carbobenzoxy-L-aspartic acidHCID 1371428250,7%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

Eight grams of DL-phenylalanine, 10 g of N-carbobenzoxy-L-aspartic acid and 2.4 g of sulfuric acid were dissolved in 90 ml of water. A 10% aqueous solution (9.7 ml) of caustic soda was added to the resulting solution over six hours while it was continuously stirred at 50° C. As a result, half of the sulfuric acid was neutralized, and the molar amount of the remaining sulfuric acid was a quarter of the amount of DL-phenylalanine. (It will be noted that in the other examples also, the amount of sulfuric acid was adjusted to be one mol per 2 mols of the finally present D-phenylalanine.) The resulting crystal was separated, washed with 10 ml of water and dried to give 8.2 g of L-phenylalanine/N-carbobenzoxy-L-aspartic acid salt. An analysis revealed that the optical purity of the L-phenylalanine contained in this salt was 98%. The molar ratio of L-phenylalanine to N-carbobenzoxy-L-aspartic acid contained in this salt was 1:1.5. An X-ray diffraction pattern of this salt in powder form had peaks at 2θ=4, 16.2, 17.4, 17.6, 18.6, 19.1, 24.6 and 28.8 (degrees).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04610827
Quelldatensatzuspto-grants-1986_09
ORD IDord-fc11b455a0314aad9f6b2359a52efcad
Quellennotizuspto-grants-1986_09