참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sulfuric Acid | HCID 1118 | — |
| 반응물 | (2R,3R,4S,5S)-2,3,4,5-tetrahydroxyhexanal | HCID 19233 | — |
| 반응물 | Naringin | HCID 442428 | — |
| 생성물 | (2R,3R,4S,5S)-2,3,4,5-tetrahydroxyhexanal | HCID 19233 | — |
| 생성물 | (2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal | HCID 107526 | — |
| 생성물 | Naringenin | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05008381 |
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| 출처 데이터셋 | uspto-grants-1991_04 |
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| ORD ID | ord-96992cd0460d4821a7e04f223c411f72 |
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| 출처 메모 | uspto-grants-1991_04 |
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