HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1698769Erstellt: 24. Oktober 2026
Potassium Carbonate → (R)-2-((tert-Butoxycarbonyl)amino)-3-((2-nitrophenyl)amino)propanoic acid
https://huagongshe.com/de/reaction/1698769
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 1-Fluoro-2-nitrobenzene | HCID 73895 | — |
| Edukt | 3-Amino-N-(tert-butoxycarbonyl)-D-alanine | HCID 7020984 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | (R)-2-((tert-Butoxycarbonyl)amino)-3-((2-nitrophenyl)amino)propanoic acid | HCID 54512598 | 99% |
Reaktionsschritte
To a solution of 2-fluoronitrobenzene (3.45 g) in N,N-dimethylformamide (60 mL), (R)-(−)-2-tert-butoxycarbonylamino-3-amino-propionic acid (5 g) and potassium carbonate (6.77 g) were added, followed by stirring overnight at 70° C. The reaction mixture was allowed to cool down, poured into ice water, and then extracted with ethyl acetate. After 1 N hydrochloric acid was added to the aqueous layer to adjust pH to 3, the aqueous layer was extracted with ethyl acetate. The organic layer was washed with brine and dried over anhydrous sodium sulfate. The solvent was then evaporated under reduced pressure. n-Hexane was added to the residue to for crystallization. The resultant crystals were collected by filtration, whereby the title compound (7.9 g) was obtained. Yield: 99%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06344452B1 |
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| Quelldatensatz | uspto-grants-2002_02 |
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| ORD ID | ord-19f5d793898a4c83b763ac3eed7429f5 |
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| Quellennotiz | uspto-grants-2002_02 |
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