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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275650Generated: October 25, 2026

(2R,3S,4S,5R)-2,3,4,5,6-pentahydroxyhexanal → aldehydo-D-Xylose

https://huagongshe.com/reaction/275650

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2R,3S,4S,5R)-2,3,4,5,6-pentahydroxyhexanalHCID 3037556—
Reactantaldehydo-L-arabinoseHCID 5460291—
Productaldehydo-D-XyloseHCID 644160—

Reaction Steps

In a preferred embodiment, the mixture fed onto the SMB comprises from about 5 wt. % to about 85 wt. % of a mixture of D-xylose and L-arabinose. Still further, the at least two components fed onto the SMB comprise D-xylose and L-arabinose. Still further, after the separation step L-arabinose is present in one eluent fraction at from about 85 wt. % to about 100 wt. %. Still further preferably, minor components, eg., galactose, are allowed to go into the D-xylose fraction, thereby providing an L-arabinose fraction comprised from about 85 wt % to about 100 wt % L-arabinose. In a separate embodiment, minor components, eg., galactose, are allowed to go with the L-arabinose fraction, thereby providing a D-xylose fraction comprised from about 85 wt. % to about 100 wt. % D-xylose. Still further, it is preferred that the D-xylose fraction is comprised of from about 85 wt. % to about 100 wt. % D-xylose. Those skilled in the art will recognize that these fractions can be additionally purified by crystallization.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06352845B1
Source datasetuspto-grants-2002_03
ORD IDord-8fc5f5d4ad7f4294aff4baec1183f6f4
Source noteuspto-grants-2002_03