HuagongsheHuagongshe Chemistry Print Report · For research reference only
[1-(3,5-Dibenzyloxybenzyl)-4-phenyl-3-pyrrolyl]methanol → 1-(3,5-Dibenzyloxybenzyl)-4-phenylpyrrole-3-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | [1-(3,5-Dibenzyloxybenzyl)-4-phenyl-3-pyrrolyl]methanol | HCID 23024986 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(3,5-Dibenzyloxybenzyl)-4-phenylpyrrole-3-carbaldehyde | HCID 23025068 | 97.5% |
Reaction Steps
A mixture of [1-(3,5-dibenzyloxybenzyl)-4-phenyl-3-pyrrolyl]methanol (23.8 g), activated manganese dioxide (50.00 g), and tetrahydrofuran (200 ml) was stirred at room temperature for two hours. After the manganese dioxide was removed by filtration, the filtrate was concentrated. The colorless crystals obtained were collected by filtration to yield 1-(3,5-dibenzyloxybenzyl)-4-phenylpyrrole-3-carbaldehyde (23.10 g, yield: 97%). This was recrystallized from tetrahydrofuran-hexane. Melting point: 117–118° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07179823B1 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-6e398ebc86d647c29c5ca98b1aa5bc2d |
| Source note | uspto-grants-2007_02 |