HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 394005Erstellt: 25. Oktober 2026
N-(tert-butoxycarbonyl)glycine → Ethyl 3-(2-{(tert-butoxycarbonyl)amino}acetylamino)propionate
https://huagongshe.com/reaction/394005
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | N-(tert-butoxycarbonyl)glycine | HCID 78288 | — |
| Edukt | beta-Alanine, ethyl ester, hydrochloride | HCID 458475 | — |
| Edukt | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Edukt | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Lösungsmittel | Triethylamine | HCID 8471 | — |
| Produkt | Ethyl 3-(2-{(tert-butoxycarbonyl)amino}acetylamino)propionate | HCID 21893946 | 75,1% |
Reaktionsschritte
To a solution of 1.5 g of ethyl 3-aminopropionate monohydrochloride and 1.7 g of 2-{(tert-butoxycarbonyl)amino}acetic acid in 50 ml of chloroform, 1.6 g of 1-hydroxybenzotriazole monohydrate, 2.3 g of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide monohydrochloride and 1.4 ml of triethylamine were added at room temperature by the order stated, and stirred for 2 hours at the same temperature. The reaction liquid was diluted with chloroform, and washed successively with saturated aqueous sodium bicarbonate solution, 10% aqueous citric acid solution and saturated saline solution, by the order stated, and dried on anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the resultant residue was purified by means of silica gel column chromatography (eluting solvent: hexane/ethyl acetate=1/4) to provide 2.0 g of the title compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06809108B1 |
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| Quelldatensatz | uspto-grants-2004_10 |
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| ORD ID | ord-ccd09b6f84ba4a99937a316e7c400846 |
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| Quellennotiz | uspto-grants-2004_10 |
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