HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 4432Erstellt: 24. Oktober 2026
L-Aspartic Acid → N-(tert-butoxycarbonyl)-L-aspartic acid
https://huagongshe.com/de/reaction/4432
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | L-Aspartic Acid | HCID 5960 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Tert-butyl 1,2,2,2-tetrachloroethyl Carbonate | HCID 2724535 | — |
| Edukt | 1,4-Dioxane--water (1/1) | HCID 21886435 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | N-(tert-butoxycarbonyl)-L-aspartic acid | HCID 99718 | 60% |
Reaktionsschritte
To a solution of 1.33 g (10 mmol) of L-aspartic acid in a dioxane/water (1:1) mixture (30 ml), 4.2 ml (30 mmol) of triethylamine are added, and the mixture is stirred until solution is complete (approximately 10 min). 2.85 g (10 mmol) of tert-butyl 1,2,2,2-tetrachloroethyl carbonate are then added and the mixture is stirred for 6 hours at 20° C. 50 ml of water are then added and the mixture is extracted with 2×20 ml of ethyl acetate. The aqueous phase is acidified (pH 2-3) with NHCl, and then extracted with 3×30 ml of ethyl acetate. The extract is washed with saturated NaCl solution, dried over MgSO4 and evaporated. The product obtained is crystallised in ethyl acetate and petroleum ether. 1.4 g (60% yield) of the expected acid is obtained. ##STR60##
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04725680 |
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| Quelldatensatz | uspto-grants-1988_02 |
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| ORD ID | ord-0c0661338a584907b09ee85e49489e40 |
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| Quellennotiz | uspto-grants-1988_02 |
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