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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1482152Generated: October 31, 2026

N-Acetyl-D-Glucosamine → D-Glucosamine

https://huagongshe.com/reaction/1482152

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Acetyl-D-GlucosamineHCID 439174—
Reactant(3R,4R,5S,6R)-3-amino-6-(hydroxymethyl)oxane-2,4,5-triol hydrochlorideHCID 2723635—
SolventWaterHCID 962—
ProductD-GlucosamineHCID 439213—

Reaction Steps

The synthesis of N-acetyl-D-glucosamine from D-glucosamine hydrochloride was performed in a single synthetic step as previously described (Zhu, et al. J Org Chem 71, 466-479, the method of which is herein incorporated by reference). Briefly, to a solution of the D-glucosamine hydrochloride salt (150 mg, 0.6 mmol) in water was added Dowex 200-400 mesh (OH—) anion-exchange resin and the pH was adjusted to 7.5. The resin was removed by filtration, yielding a D-glucosamine solution in 6 mL of water. To this solution was added 13C2-sodium acetate (1.1 eq, Cambridge Isotope Laboratories) as a pre-dissolved solution in water and 2-ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline (1.1 eq) as a pre-dissolved solution in 10 mL ethanol. The total reaction volume was brought to 40 mL by addition of ethanol. The reaction was covered in foil and stirred for 36 h at RT. This reaction was repeated using 1-13C,15N-D glucosamine hydrochloride (Isotech) as the starting material. After ethanol evaporation under reduced pressure, the crude products were purified by silica gel chromatography using a 10:4:3 mixture of ethyl acetate:pyridine:water, dried, filtered, lyophilized and stored at −20° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09410966B2
Source datasetuspto-grants-2016_08
ORD IDord-aa550a5b5abc411b8ae9402093ee2cf7
Source noteuspto-grants-2016_08