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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 324763Erstellt: 25. Oktober 2026

2-Acetylnaphthalene → (S)-(-)-1-(2-Naphthyl)ethanol

https://huagongshe.com/reaction/324763

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-AcetylnaphthaleneHCID 7122—
Eduktalpha-Methylnaphthalene-2-methanolHCID 98243—
Edukt(R)-(+)-1-(2-Naphthyl)ethanolHCID 6976569—
Produkt(S)-(-)-1-(2-Naphthyl)ethanolHCID 697656850%

Reaktionsschritte

In Example 3, the biochemical conversion reaction of immobilized buckwheat protein for the substrate (±)-1-(2-naphthyl)ethanol (200 mg) required 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% and optical purity of 99% e.e. or higher. In Example 4, as a result of reacting with the substrate (±)-1-(2-naphthyl)ethanol by continuously recycling immobilized buckwheat protein used in this fourth step from the third step, optically active (S)-1-(2-naphthyl)ethanol was obtained at an optical purity of 99% e.e. or higher by going through a conversion mechanism which sterically selectively converts (R)-1-(2-naphthyl)ethanol to 2-acetonaphthone in the same manner as the first round. Continuous recycling of immobilized buckwheat protein maintained effectiveness for at least three rounds, and there were no changes observed in reaction time, chemical yield or optical purity.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06218581B1
Quelldatensatzuspto-grants-2001_04
ORD IDord-69ead8351f1646579ec752a26ae87b6d
Quellennotizuspto-grants-2001_04