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HRID 437261생성일: 2026년 10월 23일

L-Mannose → (2R,3S,4S,5R)-2,3,4,5,6-pentahydroxyhexanal

https://huagongshe.com/ko/reaction/437261

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참여 물질

역할이름HCID투입량
반응물L-MannoseHCID 82308—
반응물GlyTouCan:G06186NUHCID 10954115—
생성물(2R,3S,4S,5R)-2,3,4,5,6-pentahydroxyhexanalHCID 3037556—

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It is also known that both D-glucose and D-mannose can be epimerized in an aqueous solution containing about 17% by weight of D-glucose or D-mannose, based on total solution weight (i.e., 20% by weight of glucose, based on the weight of water) and a small amount of molybdic acid catalyst producing a solution containing 25 percent D-mannose, remainder D-glucose on the dry basis. This epimerization is described by V. Bilik, Chem. Zvesti, 26, 183-186 (1972) and in Czech patent 149,051 (June 15, 1973). No reaction took place when sodium molybdate was used as the catalyst. Bilik and co-workers have also found that various other sugars can be epimerized in the presence of molybdate ions in aqueous solution. For example, D-fructose gives a mixture of D-sorbose, D-tagatose, and D-psicose, and sucrose gives a mixture of D-mannose and D-sorbose in a similar reaction. [Chemical Abstracts, 80, 146433s (1974)]. Also, L-arabinose gives a mixture of L-arabinose and L-ribose [Czechoslovakian Patent 149,472, July 15, 1973; C.A. 81, 78189k (1974)]; L-mannose gives a mixture of L-glucose and L-mannose [C.A. 81, 91887f (1974)]; and D-galactose gives a mixture of D-talose and D-gulose in addition to D-galactose [C.A. 81, 152523h (1974)].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04029878
출처 데이터셋uspto-grants-1977_06
ORD IDord-f7dcd13160d44e719f3eb36d3ecd39f8
출처 메모uspto-grants-1977_06