HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(Hydroxymethyl)-6-(4-nitrophenoxy)oxane-3,4,5-triol → 4-Aminophenyl glucoside
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(Hydroxymethyl)-6-(4-nitrophenoxy)oxane-3,4,5-triol | HCID 259380 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | 4-Aminophenyl glucoside | HCID 88702 | 80% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07196178B2 |
| Source dataset | uspto-grants-2007_03 |
| ORD ID | ord-8ba473a36d854cb5bf97c4fdb34ec01f |
| Source note | uspto-grants-2007_03 |