HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 2-acetyl-3-hydroxy-5-methylphenyl 2,3,4,6-tetra-O-acetyl-5-thio-beta-D-glucopyranoside
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | 3,5-Dihydroxy-4-acetyltoluene | HCID 10419531 | — |
| Reactant | 2,3,4,6-tetra-O-acetyl-5-thio-glucopyranose | HCID 11646270 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-acetyl-3-hydroxy-5-methylphenyl 2,3,4,6-tetra-O-acetyl-5-thio-beta-D-glucopyranoside | HCID 69201801 | 29.1% |
Reaction Steps
2,3,4,6-Tetra-O-acetyl-5-thio-D-glucopyranose (200 mg, 0.55 mmol), 2-acetyl-5-methylresorcinol (182 mg, 1.10 mmol), triphenylphosphine (288 mg, 1.10 mmol) and toluene (2 mL) were mixed, and to the resulting mixture, diisopropyl azodicarboxylate (40% in toluene, 555 mg) was then slowly added dropwise in ice. After stirring at room temperature for 18 hours, the reaction mixture was concentrated and the resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=70:30-50:50) to give 2-acetyl-3-hydroxy-5-methylphenyl 2,3,4,6-tetra-O-acetyl-5-thio-β-D-glucopyranoside (82 mg, 28%) as a light-yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07414072B2 |
| Source dataset | uspto-grants-2008_08 |
| ORD ID | ord-9dc73a3dcffa4dd8914d7e9f28435303 |
| Source note | uspto-grants-2008_08 |