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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1422298Erstellt: 26. Oktober 2026

(R)-2-Bromo-3-phenylpropionic acid → (S)-2-acetylthio-3-phenylpropanoic acid

https://huagongshe.com/reaction/1422298

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(R)-2-Bromo-3-phenylpropionic acidHCID 11746403—
EduktPotassium ethanethioateHCID 23670855—
KatalysatorTrioctylmethylammonium chlorideHCID 21218—
LösungsmittelEthyl AcetateHCID 8857—
Produkt(S)-2-acetylthio-3-phenylpropanoic acidHCID 10176891—

Reaktionsschritte

In a 3 l-jacketed reactor, with mechanical stirring, refrigerator and thermometer, (R)-2-bromo-3-phenyl-propionic acid (385.8 g, 1.68 moles), ethyl acetate (1,143 ml) and ALIQUAT 336° (4.2 g, 0.01 mole) were charged at 15° C. under nitrogen flow. The mixture temperature was brought to 0° C. and potassium thioacetate (222 g, 1.944 moles) was added in two portions. The reaction temperature was kept at 15° C. for 6 hours, then the mixture was twice washed with an aqueous solution of sodium thiosulfate pentahydrate (84.6 g in 820 ml of water over-all), then twice with demineralized water (600 ml total). The phases were separated and the organic one was concentrated under vacuum in a thermostated bath at 35-40° C. The resulting organic solution was cooled and filtered over celite, then added with ethyl acetate (600 ml). On the basis of the HPLC analysis, the yield in solution was equal to 87%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06080881
Quelldatensatzuspto-grants-2000_06
ORD IDord-978049f1b20247c99f74fde8785d163b
Quellennotizuspto-grants-2000_06