HuagongsheHuagongshe Chemistry Print Report · For research reference only
P-Chloroacetophenone → (1R)-1-(4-chlorophenyl)ethan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | P-Chloroacetophenone | HCID 7467 | — |
| Reactant | Benzenemethanol, 4-chloro-alpha-methyl- | HCID 18825 | — |
| Reactant | (1S)-1-(4-chlorophenyl)ethan-1-ol | HCID 6950175 | — |
| Product | (1R)-1-(4-chlorophenyl)ethan-1-ol | HCID 643324 | 51% |
Reaction Steps
As shown here, the biochemical conversion reaction of immobilized soy bean protein for the substrate (±)-1-(4-chlorophenyl)ethanol (200 mg) requires 3 days by going through bioconversion to 4-chloroacetophenone accompanying sterically selective oxidation of (S)-1-(4-chlorophenyl)ethanol to obtain 102 mg of (R)-1-(4-chlorophenyl)ethanol at a yield of 51%. Optical purity was obtained at 96% e.e.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06218581B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-0d88717d7caf44edbf9e3695a9a8c09f |
| Source note | uspto-grants-2001_04 |