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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2253249Generated: October 30, 2026

Methanol → methyl L-xylofuranoside

https://huagongshe.com/reaction/2253249

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantL-XyloseHCID 95259—
SolventHydrochloric AcidHCID 313—
Productmethyl L-xylofuranosideHCID 12042993—

Reaction Steps

This compound is prepared according to the procedure described in J. Med. Chem. 41: 3865 (1998). L-Xylose is stirred in 0.5N HCl in anhydrous MeOH for 5-10 h at room temperature. The reaction mixture is neutralized with Amberlite IRA-400 OH or Dowex—X200 anion exchange resin. The resin is removed by filtration. The combined filtrate and washings are concentrated to an oil which is subjected to column chromatography on silica gel using a mixture of CH2Cl2 and MeOH as the eluent to afford compound 1-1 as an α/β anomeric mixture.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07323449B2
Source datasetuspto-grants-2008_01
ORD IDord-c9ed3a17d0ad461facd648fc1f007edd
Source noteuspto-grants-2008_01