HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 57736Erstellt: 24. Oktober 2026
Hydrochloric Acid → Diethyl 2-benzyloxycarbonylamino-2-ethoxycarbonylsuccinate
https://huagongshe.com/de/reaction/57736
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Ethyl bromoacetate | HCID 7748 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | Diethyl 2-(benzyloxycarbonylamino)malonate | HCID 259787 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Diethyl 2-benzyloxycarbonylamino-2-ethoxycarbonylsuccinate | HCID 66725114 | 87,3% |
Reaktionsschritte
A solution of diethyl 2-benzyloxycarbonylaminomalonate (50 g) in anhydrous DMF (300 mL) was added portionwise with sodium hydride (60%, 6.47 g) with ice cooling and stirring, then the mixture was stirred at room temperature for 30 minutes, and subsequently added with ethyl 2-bromoacetate (22.6 g), and the mixture was stirred overnight. The reaction mixture was poured into diluted hydrochloric acid, the mixture was extracted with ethyl acetate, and the extract was washed with saturated brine, and then dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was subjected to silica gel column chromatography, in which elution was performed with n-hexane/ethyl acetate (5:1) for purification, and then crystallized from ethyl acetate/n-hexane to obtain the title compound (46.7 g, yield: 83%) as colorless crystals.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09434737B2 |
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| Quelldatensatz | uspto-grants-2016_09 |
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| ORD ID | ord-1df646be3b4947cd9d8bb721f2ee6f82 |
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| Quellennotiz | uspto-grants-2016_09 |
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