HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzeneacetic acid, hydrazide → HCID 16075309, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzeneacetic acid, hydrazide | HCID 70301 | — |
| Reactant | HCID 11097747 | HCID 11097747 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 16075309 | HCID 16075309 | 78% |
Reaction Steps
To a solution of-phenylacetic acid hydrazide (0.24 mmol) in absolute EtOH 10 mL and acetic acid 0.4 mL is added 2-{[(4-methylphenyl)sulfonyl]methyl}benzaldehyde (0.22 mmol). The reaction is stirred at room temperate for 2.5 hr with white ppt formation. The reaction mixture is then filtered. The solid is triturated with MeOH to give N′-[(1E)-(2-{[(4-methylphenyl)sulfonyl]methyl}phenyl)methylene]-2-phenylacetohydrazide in 78% yield. 1H NMR (400 MHz, DMSO-d6) □ 11.50–11.25 (2s, 1H), 8.22–8.13 (2s, 1H), 7.79 (m, 1H), 7.56 (m, 2H), 7.31 (m, 10H), 4.93–4.80 (2s, 2H), 3.95–3.57 (2s, 2H), 2.36–2.31 (2s, 3H). ESI− for C23H22N2O3S, m/z 405 (M−H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07026339B2 |
| Source dataset | uspto-grants-2006_04 |
| ORD ID | ord-dae8af03c7dd41beba51b60bd355b820 |
| Source note | uspto-grants-2006_04 |