HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 57745Erstellt: 24. Oktober 2026
Hydrochloric Acid → Diethyl 2-benzyloxycarbonylamino-2-(benzyloxycarbonylmethyl)malonate
https://huagongshe.com/de/reaction/57745
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | Benzyl bromoacetate | HCID 62576 | — |
| Edukt | Diethyl 2-(benzyloxycarbonylamino)malonate | HCID 259787 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Diethyl 2-benzyloxycarbonylamino-2-(benzyloxycarbonylmethyl)malonate | HCID 66725163 | 99% |
Reaktionsschritte
A solution of diethyl 2-benzyloxycarbonylaminomalonate (30 g) in anhydrous DMF (100 mL) was added portionwise with sodium hydride (60%, 4.27 g) with ice cooling and stirring, then the mixture was stirred at room temperature for 30 minutes, and then added with benzyl 2-bromoacetate (28.9 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, and then purification was performed with n-hexane/ethyl acetate (4:1), to obtain the title compound (43.9 g, yield: 99%) as colorless oil.
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-602dde33759e487e961a51b22824aeaa |
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| Quellennotiz | uspto-grants-2016_09 |
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