HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Acetylnaphthalene → (S)-(-)-1-(2-Naphthyl)ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Acetylnaphthalene | HCID 7122 | — |
| Reactant | alpha-Methylnaphthalene-2-methanol | HCID 98243 | — |
| Reactant | (R)-(+)-1-(2-Naphthyl)ethanol | HCID 6976569 | — |
| Product | (S)-(-)-1-(2-Naphthyl)ethanol | HCID 6976568 | 50% |
Reaction Steps
As shown here, the biochemical conversion reaction of immobilized green pea protein for the substrate 1-(2-naphthyl)ethanol (201 mg) requires 4 days by going through bioconversion to 2-acetonaphthone accompanying sterically selective oxidation of (R)-1-(2-naphthyl)ethanol to obtain 100 mg of (S)-1-(2-naphthyl)ethanol at a yield of 50% at an optical purity of 99% e.e. or higher (see FIG. 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06218581B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-7b35a6765154448fa7d62659ae817dc6 |
| Source note | uspto-grants-2001_04 |