HuagongsheHuagongshe Chemistry Print Report · For research reference only
[3-(methylamino)-1-phenyl-1H-pyrazol-4-yl]methanol → 3-(methylamino)-1-phenyl-1H-pyrazole-4-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | [3-(methylamino)-1-phenyl-1H-pyrazol-4-yl]methanol | HCID 69217492 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(methylamino)-1-phenyl-1H-pyrazole-4-carbaldehyde | HCID 23076364 | — |
Reaction Steps
A mixture of [3-(methylamino)-1-phenyl-1H-pyrazol-4-yl]methanol (15.42 g), activated manganese dioxide (50 g) and tetrahydrofuran (150 mL) was stirred at room temperature for 16 hrs. The obtained mixture was filtered, and the filtrate was concentrated. The residue was subjected to silica gel column chromatography to give 3-(methylamino)-1-phenyl-1H-pyrazole-4-carbaldehyde as colorless crystals from a fraction eluted with ethyl acetate-hexane (1:4, v/v). Recrystallization from ethyl acetate-hexane gave colorless needle crystal (9.17 g, yield 60%). melting point: 83-84° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07368578B2 |
| Source dataset | uspto-grants-2008_05 |
| ORD ID | ord-d9459743dd9e4c50905fa4a369406992 |
| Source note | uspto-grants-2008_05 |