HuagongsheHuagongshe Chemistry Print Report · For research reference only
1H-1,2,4-Triazole → 4-(1H-1,2,4-triazol-1-yl)benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1H-1,2,4-Triazole | HCID 9257 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Fluorobenzaldehyde | HCID 68023 | — |
| Catalyst | HCID 178419072 | HCID 178419072 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 4-(1H-1,2,4-triazol-1-yl)benzaldehyde | HCID 2776488 | — |
Reaction Steps
A mixture of 1,2,4-triazole (4.06 g, 58.7 mmol), potassium carbonate (9.05 g, 65.5 mmol), 4-fluorobenzaldehyde (6.3 ml, 58.7 mmol), and copper(I) oxide (0.26 g, 1.82 mmol) in pyridine (30 ml) is heated under nitrogen atmosphere at reflux overnight. After pyridine is distilled, the residue is diluted with chloroform, filtered, and washed with chloroform. The combined filtrate is washed with water, dried over magnesium sulfate, and concentrated in vacuo. The crude material is purified by column chromatography on silica with hexane/ethyl acetate (1:2) to give 4-(1,2,4-triazol-1-yl)-benzaldehyde and with ethyl acetate/methanol (19:1) to give 4-(1,3,4-triazol-1-yl)-benzaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05703106 |
| Source dataset | uspto-grants-1997_12 |
| ORD ID | ord-98f2a17d58444bc39103f80ee88276d3 |
| Source note | uspto-grants-1997_12 |