HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-(4-Tolyl)-3-(4-nitrophenyl)-5-aminopyrazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | o-Tolylhydrazine | HCID 68256 | — |
| Reactant | 4-Nitrobenzoylacetonitrile | HCID 591459 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(4-Tolyl)-3-(4-nitrophenyl)-5-aminopyrazole | HCID 12018677 | — |
Reaction Steps
To a solution of 2-cyano-4′nitroacetophenone in ethanol (100 mL) at room temperature was added tolylhydrazine (6.44 g, 0.04 mol) and triethylamine (15.4 mL, 0.11 mol). The resulting solution was heated to reflux and maintained at reflux for 1 h. The solution was cooled to room temperature at which time EtOAc (500 mL) was added. The organic solution was washed with brine (2×500 mL), dried over Na2SO4 and concentrated by rotary evaporation. The residue was purified by column chromatography on silica gel eluting with 1:1 hexane/EtOAc to yield 1-(4-tolyl)-3-(4-nitrophenyl)-5-aminopyrazole as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06531478B2 |
| Source dataset | uspto-grants-2003_03 |
| ORD ID | ord-4da161b0cc6e4e3dbfe5cadb98633822 |
| Source note | uspto-grants-2003_03 |