HuagongsheHuagongshe Chemistry Print Report · For research reference only
(3-benzyloxy-1-methyl-1H-pyrazol-4-yl)methanol → 3-(benzyloxy)-1-methyl-1H-pyrazole-4-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (3-benzyloxy-1-methyl-1H-pyrazol-4-yl)methanol | HCID 22930776 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(benzyloxy)-1-methyl-1H-pyrazole-4-carbaldehyde | HCID 22930723 | 81.2% |
Reaction Steps
A mixture of (3-benzyloxy-1-methyl-1H-pyrazol-4-yl)methanol (18.40 g), active manganese dioxide (40.00 g) and tetrahydrofuran (200 ml) was stirred at room temperature for 9 hrs. Manganese dioxide was filtered off and the filtrate was concentrated. The residue was subjected to silica gel column chromatography, and 3-benzyloxy-1-methyl-1H-pyrazole-4-carbaldehyde (14.80 g, yield 81%) was obtained as a colorless oil from a fraction eluted with ethyl acetate-hexane (2:1, volume ratio).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07241785B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-94b8d23fa42d4fce93be60b37627eca5 |
| Source note | uspto-grants-2007_07 |