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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 324760Erstellt: 25. Oktober 2026

P-Chloroacetophenone → (1R)-1-(4-chlorophenyl)ethan-1-ol

https://huagongshe.com/reaction/324760

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktP-ChloroacetophenoneHCID 7467—
EduktBenzenemethanol, 4-chloro-alpha-methyl-HCID 18825—
Edukt(1S)-1-(4-chlorophenyl)ethan-1-olHCID 6950175—
Produkt(1R)-1-(4-chlorophenyl)ethan-1-olHCID 64332458%

Reaktionsschritte

As shown here, the biochemical conversion reaction of immobilized buckwheat protein for the substrate (±)-1-(4-chlorophenyl)ethanol (200 mg) requires 13 days by going through bioconversion to 4-chloroacetophenone accompanying sterically selective oxidation of (S)-1-(4-chlorophenyl)ethanol to obtain 116 mg of (R)-1-(4-chlorophenyl)ethanol at a yield of 58%. Optical purity was obtained at 91% e.e.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06218581B1
Quelldatensatzuspto-grants-2001_04
ORD IDord-038178653421481595bc61023e775d66
Quellennotizuspto-grants-2001_04