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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 346435Erstellt: 24. Oktober 2026

Phosphate → (S)-alpha-(Trifluoromethyl)benzyl alcohol

https://huagongshe.com/de/reaction/346435

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhosphateHCID 1061—
EduktIsopropanolHCID 3776—
Edukt2,2,2-TrifluoroacetophenoneHCID 9905—
LösungsmittelEthyl AcetateHCID 8857—
Produkt(S)-alpha-(Trifluoromethyl)benzyl alcoholHCID 95556—

Reaktionsbedingungen

Temperatur30 °C

Reaktionsschritte

To 0.02 g of the aforementioned wet bodies was added 500 μl of 50 mM phosphate buffer (pH 7.0) containing 1% 2,2,2-trifluoroacetophenone and 5% 2-propanol, followed by stirring at 30° C. for 18 hours. Then, after adding 500 μl of ethyl acetate to the reaction mixture, the mixture was subjected to centrifugal separation to obtain the organic phase. The organic phase was subjected to an analysis of the content by way of gas chromatography under the following condition. 2,2,2-Trifluoro-1-phenylethanol was produced at a ratio of 49.4% based on the amount of 2,2,2-trifluoroacetophenone used in the reaction. Furthermore, optical purity of 2,2,2-trifluoro-1-phenylethanol in the organic phase was measured under the following condition. The (S)-form of 99% e.e. was demonstrated.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07172894B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-3b169d156aa444c09b848c7a39e4a6d4
Quellennotizuspto-grants-2007_02