HuagongsheHuagongshe Chemistry Print Report · For research reference only
(1-benzyl-3-benzyloxy-1H-pyrazol-4-yl)methanol → 1-benzyl-3-(benzyloxy)-1H-pyrazole-4-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (1-benzyl-3-benzyloxy-1H-pyrazol-4-yl)methanol | HCID 22930765 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-benzyl-3-(benzyloxy)-1H-pyrazole-4-carbaldehyde | HCID 22930768 | 90% |
Reaction Steps
A mixture of (1-benzyl-3-benzyloxy-1H-pyrazol-4-yl)methanol (14.70 g), activated manganese dioxide (30.00 g), and tetrahydrofuran (200 ml) was stirred at room temperature for 2 hours. After the manganese dioxide was removed by filtration, the filtrate was concentrated. The crystals obtained were collected by filtration to yield 1-benzyl-3-benzyloxy-1H-pyrazole-4-carbaldehyde (13.10 g, yield: 90%). This was recrystallized from tetrahydrofuran-hexane. Melting point: 85–86° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07179823B1 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-4573e56c154348ed80950db373df823f |
| Source note | uspto-grants-2007_02 |