HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Biphenyl-2-carboxylic acid (3-trifluoromethyl-benzylidene)-hydrazide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 3-(Trifluoromethyl)benzaldehyde | HCID 67990 | — |
| Reactant | 2-Phenylbenzhydrazide | HCID 2760365 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Biphenyl-2-carboxylic acid (3-trifluoromethyl-benzylidene)-hydrazide | HCID 86587161 | 87% |
Reaction Steps
To a stirred solution of biphenyl-2-carboxylic acid-hydrazide (0.212 g, 1.0 mmol) in 20 mL EtOH was added 3-trifluoromethyl-benzaldehyde (0.174 g, 1.0 mmol) in 5 mL EtOH at room temperature. The mixture was refluxed for 4 h and cooled to room temperature, then was diluted by 100 mL of water. The precipitate was collected, washed with MeOH, and dried to yield the title compound (0.320 g, 87%). 1H NMR (acetone-d6): 11.60 (s, 1H), 7.79 (s, 1H), 7.57 (s, 1H), 7.52 (d, J=12 Hz, 1H), 7.35 (d, J=12 Hz, 1H), 6.97˜7.15 (m, 10H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07074813B2 |
| Source dataset | uspto-grants-2006_07 |
| ORD ID | ord-47adc2ac387f4000a9d9c47a18468d30 |
| Source note | uspto-grants-2006_07 |