HuagongsheHuagongshe Chemistry Print Report · For research reference only
(5-Methyl-1-trityl-1H-imidazol-4-yl)methanol → 5-methyl-1-trityl-1H-imidazole-4-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (5-Methyl-1-trityl-1H-imidazol-4-yl)methanol | HCID 11544901 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5-methyl-1-trityl-1H-imidazole-4-carbaldehyde | HCID 11824338 | 100.6% |
Reaction Steps
A mixture of 5-methyl-1-(triphenylmethyl)-1H-imidazole-4-methanol (4.0 g), manganese dioxide (activated) (40 g) and dioxan (225 ml) was stirred at room temperature overnight. The suspension was filtered through Hyflo, the solid washed with hot chloroform (1 l) and the combined filtrates evaporated in vacuo to leave an off-white solid (4.0 g). This solid was purified by FCC eluting with chloroform to give an off-white solid which was triturated with hexane (ca. 50 ml) to give the title compound (2.99 g) as a white crystalline solid, m.p. 184°-188° (decomp.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04808581 |
| Source dataset | uspto-grants-1989_02 |
| ORD ID | ord-7f5a3547c61045f0a12530e6072d03c3 |
| Source note | uspto-grants-1989_02 |