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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1085234생성일: 2026년 10월 25일

Sulfuric Acid → (2R,3R,4S,5S)-2,3,4,5-tetrahydroxyhexanal

https://huagongshe.com/reaction/1085234

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물(2R,3R,4S,5S)-2,3,4,5-tetrahydroxyhexanalHCID 19233—
반응물NaringinHCID 442428—
생성물(2R,3R,4S,5S)-2,3,4,5-tetrahydroxyhexanalHCID 19233—
생성물(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanalHCID 107526—
생성물NaringeninHCID 439246—

반응 단계

Illustrative of a process for obtaining L-rhamnose from naringin is described by G. N. Pulley, et al., "Preparation of Rhamnose from Naringin", J. Amer. Chem. Soc., 61, p. 175 (1939), in which naringin is hydrolyzed by refluxing it with sulphuric acid (~3.7%). Glucose, L-rhamnose, naringenin and other reaction products are formed by the reaction. The reaction medium is cooled and naringenin, which is semi-solid, is separated from the cooled reaction medium. The remaining filtrate then is neutralized and heated to boiling in the presence of charcoal. The charcoal treated product is concentrated in vacuo and then is inoculated with yeast to ferment glucose. L-rhamnose is isolated from the fermented liquor by several steps of concentration in vacuo and washing.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05008381
출처 데이터셋uspto-grants-1991_04
ORD IDord-96992cd0460d4821a7e04f223c411f72
출처 메모uspto-grants-1991_04