HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → N'-benzylidene-4-trifluoromethylbenzohydrazide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 4-(Trifluoromethyl)benzohydrazide | HCID 520662 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N'-benzylidene-4-trifluoromethylbenzohydrazide | HCID 6736306 | 74% |
Reaction Steps
To a solution (50 ml) of 4-trifluoromethylbenzohydrazide (3.06 g) and benzaldehyde (1.52 ml) in methanol was added dropwise conc. sulfuric acid (0.5 ml), and this mixture was stirred at room temperature for 1 hr. The reaction mixture was concentrated, and the residue was washed with hexane-ethanol (1:1, volume ratio) and recrystallized from ethanol to give N′-benzylidene-4-trifluoromethylbenzohydrazide (3.23 g, yield 74%) as colorless needle crystals. melting point: 216–217° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07223791B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-04360be69d8a45b491ff0ea21c329994 |
| Source note | uspto-grants-2007_05 |