HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 902905Erstellt: 25. Oktober 2026
D-Phenylalanine → (R)-2-Bromo-3-phenylpropionic acid
https://huagongshe.com/reaction/902905
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | D-Phenylalanine | HCID 71567 | — |
| Edukt | Potassium Bromide | HCID 253877 | — |
| Edukt | Sodium Nitrite | HCID 23668193 | — |
| Lösungsmittel | Sulfuric Acid | HCID 1118 | — |
| Produkt | (R)-2-Bromo-3-phenylpropionic acid | HCID 11746403 | 51,9% |
Reaktionsschritte
Potassium bromide (24.49 g, 0.21 moles) was first dissolved in a 2.50 N aqueous solution of sulfuric acid (120 mL). To this stirring solution was then added D-phenylalanine (10.00 g, 60.54 mmoles). After the addition, the mixture was cooled down to 0° C. and sodium nitrite (6.27 g., 90.87 mmoles) was added in small portions during 30 minutes. A strong bubbling was observed. The reaction was kept at this temperature for 50 minutes, and it was then allowed to proceed at room temperature for another 60 minutes. The crude product was isolated using standard work up and the obtained residue was purified by flash chromatography (SiO2, 30% ethyl acetate-70% hexanes) to give 7.20 g (51.9% yield) of the title compound as a yellowish oil: 1H NMR (CDCl3, 300 MHz) □ 10.86 (br s, 1H), 7.31 (m, 5H), 4.48 (t, 1H), 3.51 (dd, 1H), 3.29 (dd, 1H); 13C NMR (CDCl3, 75 MHz) □175.29, 136.26, 129.10, 128.69, 127.42, 44.83, 40.62.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07365091B2 |
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| Quelldatensatz | uspto-grants-2008_04 |
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| ORD ID | ord-7032ca5b14e5440d92c258596283f81f |
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| Quellennotiz | uspto-grants-2008_04 |
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