HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 477204Erstellt: 25. Oktober 2026
Triethylamine → Diethyl 2-[[N-(chloroacetyl)glycyl]amino]malonate
https://huagongshe.com/reaction/477204
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Edukt | N-Chloroacetylglycine | HCID 233485 | — |
| Edukt | Propanedioic acid, 2-amino-, 1,3-diethyl ester, hydrochloride (1:1) | HCID 3084143 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Diethyl 2-[[N-(chloroacetyl)glycyl]amino]malonate | HCID 15053734 | 83,5% |
Reaktionsschritte
To a suspension of diethyl 2-aminomalonate hydrochloride (4.2 g) in tetrahydrofuran are added triethylamine (2.1 g) and N-(chloroacetyl)glycine (3.0 g), and the mixture is cooled to 0° to 5° C. To the mixture is further added N,N'-dicyclohexylcarbodiimide (4.3 g), and the mixture is stirred at the same temperature for 2 hours and then allowed to stand at room temperature overnight. Insoluble substance is filtered off from the reaction mixture, and the filtrate is concentrated under reduced pressure. To the residue is added ethyl acetate, and the insoluble substance is filtered off. The filtrate is concentrated under reduced pressure, and the residue is recrystallized from ethyl acetateisopropyl ether to give diethyl 2-[[N-(chloroacetyl)glycyl]amino]malonate (5.1 g), m.p. 104.5°-105° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04886894 |
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| Quelldatensatz | uspto-grants-1989_12 |
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| ORD ID | ord-1aa171324c1d4d6abdbf3e1423e3505a |
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| Quellennotiz | uspto-grants-1989_12 |
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