Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Benzyl chloroformate | HCID 10387 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 2-Naphthylalanine | HCID 185915 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | Z-L-2-Nal-OH | HCID 7023496 | — |
Reaktionsschritte
5 g of 3-(2-naphthyl)-L-alanine and 0.93 g of sodium hydroxide in 12 ml of water were cooled to 0° C. and stirred while a solution of 1.4 g of sodium hydroxide in 9 ml of water and 5 ml of benzyl chloroformate were added simultaneously during 10 minutes. Stirring was continued for 2 hours and the mixture was allowed to come to room temperature. The mixture was diluted with water and then extracted with diethyl ether. The aqueous layer was acidified with 4 ml of concentrated hydrochloric acid and extracted with ethyl acetate. The ethyl acetate extracts were back-washed with water. The combined ethyl acetate extracts were dried over sodium sulphate, filtered, evaporated and triturated with petroleum ether (boiling point 40°-60° C.) to give 7.5 g of N-(benzyloxycarbonyl)-3-(2-naphthyl)-L-alanine of melting point 109°-111° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05620987 |
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| Quelldatensatz | uspto-grants-1997_04 |
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| ORD ID | ord-5318d758e20a4615be261e4f2dfa0958 |
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| Quellennotiz | uspto-grants-1997_04 |
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