HuagongsheHuagongshe Chemistry Print Report · For research reference only
(3-benzyloxy-1-phenyl-1H-pyrazol-5-yl)methanol → HCID 22930766, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (3-benzyloxy-1-phenyl-1H-pyrazol-5-yl)methanol | HCID 22930692 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22930766 | HCID 22930766 | 91% |
Reaction Steps
A mixture of (3-benzyloxy-1-phenyl-1H-pyrazol-5-yl)methanol (11.20 g), activated manganese dioxide (30.00 g) and tetrahydrofuran (300 mL) was stirred overnight at room temperature. The insoluble material was removed by filtration, and the mother liquid was concentrated. The residue was subjected to silica gel column chromatography to give 3-benzyloxy-1-phenyl-1H-pyrazole-5-carbaldehyde (10.10 g, yield 91%) as a pale-yellow oil from a fraction eluted with ethyl acetate-hexane (1:2, v/v).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07368578B2 |
| Source dataset | uspto-grants-2008_05 |
| ORD ID | ord-4e3ba7244554440e8361a27aae44d5df |
| Source note | uspto-grants-2008_05 |