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HRID 324763作成日:2026年10月26日

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

https://huagongshe.com/reaction/324763

反応式

関与物質

役割名称HCID仕込み量
反応物2-AcetylnaphthaleneHCID 7122—
反応物alpha-Methylnaphthalene-2-methanolHCID 98243—
反応物(R)-(+)-1-(2-Naphthyl)ethanolHCID 6976569—
生成物(S)-(-)-1-(2-Naphthyl)ethanolHCID 697656850%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06218581B1
出典データセットuspto-grants-2001_04
ORD IDord-69ead8351f1646579ec752a26ae87b6d
出典メモuspto-grants-2001_04