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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085234Generated: October 25, 2026

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

https://huagongshe.com/reaction/1085234

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactant(2R,3R,4S,5S)-2,3,4,5-tetrahydroxyhexanalHCID 19233—
ReactantNaringinHCID 442428—
Product(2R,3R,4S,5S)-2,3,4,5-tetrahydroxyhexanalHCID 19233—
Product(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanalHCID 107526—
ProductNaringeninHCID 439246—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05008381
Source datasetuspto-grants-1991_04
ORD IDord-96992cd0460d4821a7e04f223c411f72
Source noteuspto-grants-1991_04