HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Nitroacetophenone → (1S)-1-(4-nitrophenyl)ethan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Nitroacetophenone | HCID 7487 | — |
| Reactant | 1-(4-Nitrophenyl)ethan-1-ol | HCID 592376 | — |
| Reactant | (R)-1-(4-nitrophenyl)ethanol | HCID 9793932 | — |
| Product | (1S)-1-(4-nitrophenyl)ethan-1-ol | HCID 9815318 | 25% |
Reaction Steps
As shown here, the biochemical conversion reaction of immobilized buckwheat protein for the substrate (±)-1-(4-nitrophenyl)ethanol (200 mg) requires 17 days by going through bioconversion to 4-nitroacetophenone accompanying sterically selective oxidation of (R)-1-(4-nitrophenyl)ethanol to obtain 50 mg of (S)-1-(4-nitrophenyl)ethanol at a yield of 25%. Optical purity was obtained at 99% e.e.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06218581B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-bf43e5408abb474dba61a8b0864fce62 |
| Source note | uspto-grants-2001_04 |