HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 57744Erstellt: 24. Oktober 2026
Hydrochloric Acid → Diethyl 2-benzyloxycarbonylamino-2-(t-butoxycarbonylmethyl)malonate
https://huagongshe.com/de/reaction/57744
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | tert-Butyl bromoacetate | HCID 79177 | — |
| Edukt | Diethyl 2-(benzyloxycarbonylamino)malonate | HCID 259787 | — |
| Katalysator | Potassium Iodide | HCID 4875 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Diethyl 2-benzyloxycarbonylamino-2-(t-butoxycarbonylmethyl)malonate | HCID 66725345 | 100,8% |
Reaktionsschritte
A suspension of diethyl 2-benzyloxycarbonylaminomalonate (5.0 g), potassium carbonate (2.7 g), potassium iodide (0.27 g), and t-butyl 2-bromoacetate (4.1 g) in DMF (50 mL) was stirred at 50° C. for 1 hour. The reaction mixture was cooled, and then 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 (5:1), to obtain the title compound (6.9 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-90797a7338924070b568b0d13d20c8a2 |
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| Quellennotiz | uspto-grants-2016_09 |
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