HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Nitroacetophenone → (R)-1-(4-nitrophenyl)ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Nitroacetophenone | HCID 7487 | — |
| Reactant | 1-(4-Nitrophenyl)ethan-1-ol | HCID 592376 | — |
| Reactant | (1S)-1-(4-nitrophenyl)ethan-1-ol | HCID 9815318 | — |
| Product | (R)-1-(4-nitrophenyl)ethanol | HCID 9793932 | 38% |
Reaction Steps
As shown here, the biochemical conversion reaction of immobilized green pea protein for the substrate (±)-1-(4-nitrophenyl)ethanol (200 mg) requires 4 days by going through bioconversion to 4-nitroacetophenone accompanying sterically selective oxidation of (S)-1-(4-nitrophenyl)ethanol to obtain 76 mg of (R)-1-(4-nitrophenyl)ethanol at a yield of 38%. Optical purity was obtained at 54% e.e. HPLC conditions were set at a flow rate of 0.5 ml/min, while GC conditions were set to an oven temperature of 190° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06218581B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-75d1154ef2104dab9d1ede9d228ef9c2 |
| Source note | uspto-grants-2001_04 |