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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 407185생성일: 2026년 10월 25일

Potassium Chloride → (3S)-4,4-Dimethoxytetrahydro-2H-pyran-3-ol

https://huagongshe.com/reaction/407185

반응식

참여 물질

역할이름HCID투입량
반응물Potassium ChlorideHCID 4873—
반응물NADP nicotinamide-adenine-dinucleotide phosphateHCID 5886—
반응물AcetonitrileHCID 6342—
반응물(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanalHCID 107526—
용매TolueneHCID 1140—
생성물(3S)-4,4-Dimethoxytetrahydro-2H-pyran-3-olHCID 66979040—

반응 조건

온도30 °C

반응 단계

The above organic solution of 4,4-dimethoxydihydro-2H-pyran-3(4H)-one was extracted 3× with phosphate buffered water (0.55 L). To the combined aqueous extracts was added D-glucose (180 g, 100 mmol), and the solution was heated to 30° C. When the solution exceeded 27° C. upon heating B-NADP+ (1.60 g, 499 mmol) GDH-103 (1.60 g, 499 mmol) and KRED-130 (1.60 g, 499 mmol) were added and the mixture was stirred for 17 h at 30° C. Potassium chloride (200 g, 2.68 mol) and acetonitrile (1.3 L) were added. After 30 min, the reaction mixture was transferred to 6 L sep funnel and additional MeCN (0.67 L) and toluene (0.87 L) were added. The aqueous layer was back extracted 1× with a mixture of acetonitrile (1.95 L) and toluene (0.65 L), and 1× with acetonitrile (1.5 L). The combined organic extracts were concentrated in vacuo to provide (3S)-4,4-dimethoxytetrahydro-2H-pyran-3-ol.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08754220B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-465ab4cef5d84f668b3fc22ca4efe57f
출처 메모uspto-grants-2014_06