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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 324763생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/324763

반응식

참여 물질

역할이름HCID투입량
반응물2-AcetylnaphthaleneHCID 7122—
반응물alpha-Methylnaphthalene-2-methanolHCID 98243—
반응물(R)-(+)-1-(2-Naphthyl)ethanolHCID 6976569—
생성물(S)-(-)-1-(2-Naphthyl)ethanolHCID 697656850%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06218581B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-69ead8351f1646579ec752a26ae87b6d
출처 메모uspto-grants-2001_04