HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
P-Chloroacetophenone → (1R)-1-(4-chlorophenyl)ethan-1-ol
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | P-Chloroacetophenone | HCID 7467 | — |
| Edukt | Benzenemethanol, 4-chloro-alpha-methyl- | HCID 18825 | — |
| Edukt | (1S)-1-(4-chlorophenyl)ethan-1-ol | HCID 6950175 | — |
| Produkt | (1R)-1-(4-chlorophenyl)ethan-1-ol | HCID 643324 | 58% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06218581B1 |
| Quelldatensatz | uspto-grants-2001_04 |
| ORD ID | ord-038178653421481595bc61023e775d66 |
| Quellennotiz | uspto-grants-2001_04 |