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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 902905Erstellt: 25. Oktober 2026

D-Phenylalanine → (R)-2-Bromo-3-phenylpropionic acid

https://huagongshe.com/reaction/902905

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktD-PhenylalanineHCID 71567—
EduktPotassium BromideHCID 253877—
EduktSodium NitriteHCID 23668193—
LösungsmittelSulfuric AcidHCID 1118—
Produkt(R)-2-Bromo-3-phenylpropionic acidHCID 1174640351,9%

Reaktionsbedingungen

Temperatur0 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07365091B2
Quelldatensatzuspto-grants-2008_04
ORD IDord-7032ca5b14e5440d92c258596283f81f
Quellennotizuspto-grants-2008_04