HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyrazole → 4-(1H-Pyrazol-1-yl)benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyrazole | HCID 1048 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 4-Formylphenylboronic Acid | HCID 591073 | — |
| Catalyst | Cupric acetate | HCID 8895 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-(1H-Pyrazol-1-yl)benzaldehyde | HCID 2776477 | 66.9% |
Reaction Steps
Copper acetate (91 mg, 0.5 mmol), pyridine (53 mg, 0.67 mmol) and active Molecular Sieve 4A (250 mg) were added to a solution of 4-formylphenylboronic acid (100 mg, 0.67 mmol) and pyrazole (16 mg, 0.33 mmol) in 1,4-dioxane (4 ml), and they were stirred at room temperature for 72 hours. The reaction mixture was filtered through Celite, and the obtained filtrate was concentrated and then purified by the silica gel TLC chromatography to obtain 1-(4-formylphenyl)pyrazole (yield: 38 mg, 66%) in the form of a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07632830B2 |
| Source dataset | uspto-grants-2009_12 |
| ORD ID | ord-e9a4a07c76424f88a6b0f4fb96006c78 |
| Source note | uspto-grants-2009_12 |