HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Water → N-(Benzyloxycarbonyl)-L-aspartyl-L-phenylalanine methyl ester
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Sodium Acetate | HCID 517045 | — |
| Edukt | (S)-Benzyl (tetrahydro-2,5-dioxo-3-furyl)carbamate | HCID 11128682 | — |
| Edukt | L-phenylalanine methyl ester sulfate | HCID 20841682 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Produkt | N-(Benzyloxycarbonyl)-L-aspartyl-L-phenylalanine methyl ester | HCID 10159630 | 73,1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05302743 |
| Quelldatensatz | uspto-grants-1994_04 |
| ORD ID | ord-a893da5500e64c718ebcd50755c54d72 |
| Quellennotiz | uspto-grants-1994_04 |