HuagongsheHuagongshe Chemistry Print Report · For research reference only
[5-(Benzyloxy)-3-methyl-1-benzofuran-2-yl]methanol → 5-(Benzyloxy)-3-methyl-1-benzofuran-2-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | [5-(Benzyloxy)-3-methyl-1-benzofuran-2-yl]methanol | HCID 66778297 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-(Benzyloxy)-3-methyl-1-benzofuran-2-carbaldehyde | HCID 86662753 | 96.4% |
Reaction Steps
To a solution (30 mL) of [5-(benzyloxy)-3-methyl-1-benzofuran-2-yl]methanol (2.8 g) synthesized in the above-mentioned (2) in toluene was added manganese dioxide (5 g), and the mixture was heated under reflux with a Dean-Stark trap for 1 hr. The reaction mixture was allowed to cool to room temperature, catalyst was filtered through celite. The filtrate was concentrated under reduced pressure to give the title object compound (2.68 g, 94%) as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08436043B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-db20419ce3e349ce9c6ad723b9299081 |
| Source note | uspto-grants-2013_05 |