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 | Methyl L-phenylalaninate hydrochloride | HCID 75736 | — |
| Edukt | Sodium Acetate | HCID 517045 | — |
| Edukt | (S)-Benzyl (tetrahydro-2,5-dioxo-3-furyl)carbamate | HCID 11128682 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Produkt | N-(Benzyloxycarbonyl)-L-aspartyl-L-phenylalanine methyl ester | HCID 10159630 | 70,1% |
Reaktionsschritte
In 100.4 g of acetic acid, 25.1 g (0.1 mole) of N-benzyloxycarbonyl-L-aspartic anhydride was suspended and 21.6 g (0.1 mole) of L-phenylalanine methyl ester hydrochloride was added at 10°-15° C. Successively 9.2 g (0.11 mole) of sodium acetate was added over 30 minutes at the same temperature. The reaction was carried out for 3 hours with stirring at the same temperature. Thereafter 75.3 g of water was added and cooled 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 30.0 g (70.1% yield on L-phenylalanine methyl ester hydrochloride).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05302743 |
| Quelldatensatz | uspto-grants-1994_04 |
| ORD ID | ord-7b73544978204f3ba8f8803bbe568f34 |
| Quellennotiz | uspto-grants-1994_04 |