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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460421Generated: October 27, 2026

2-(Hydroxymethyl)-6-(4-nitrophenoxy)oxane-3,4,5-triol → 4-Aminophenyl glucoside

https://huagongshe.com/reaction/460421

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Hydroxymethyl)-6-(4-nitrophenoxy)oxane-3,4,5-triolHCID 259380—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventMeOH tetrahydrofuranHCID 21899815—
Product4-Aminophenyl glucosideHCID 8870280%

Reaction Steps

p-nitrophenyl-β-D-glucopyranoside (Tokyo Chemical Industries) (250 mg) was dissolved in a methanol/tetrahydrofuran mixed solvent (20 ml/5 ml), and 10% palladium carbon (250 mg) was added to this solution. Hydrogen gas was introduced under a nitrogen gas atmosphere into the reaction solution at room temperature for 3 hours. The reaction mixture was filtered to remove palladium carbon, the filtrate was evaporated under vacuum, and solidified. This residue was purified by silica gel chromatography using a tetrahydrofuran/chloroform mixed solvent (1/1, volume ratio) as an eluant, and p-aminophenol-β-D-glucopyranoside was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07196178B2
Source datasetuspto-grants-2007_03
ORD IDord-8ba473a36d854cb5bf97c4fdb34ec01f
Source noteuspto-grants-2007_03