HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Hydroxybenzoic acid hydrazide → 4-Hydroxy-N'-[(4-methoxyphenyl)methylidene]benzohydrazide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Hydroxybenzoic acid hydrazide | HCID 1742 | — |
| Reactant | 4-Methoxybenzaldehyde | HCID 31244 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Hydroxy-N'-[(4-methoxyphenyl)methylidene]benzohydrazide | HCID 310068 | 94.3% |
Reaction Steps
To a solution of 4-hydroxybenzhydrazide (0.3 g, 0.002 mol) and p-anisaldehyde (0.27 g, 0.002 mol) in abs. EtOH (10 mL) was added 1 drop of acetic acid. The reaction mixture was refluxed for 4 hours. The reaction mixture was cooling to room temperature and concentrated to remove solvent. The resulting residue was solidified by EtOAc to give white solid 0.51 g, in 93% yield, mp: 209.0° C. 1H NMR (CD3OD) δ 8.23 (s, 1H), 7.82 (d, 2H), 7.76 (d, 2H), 6.97 (d, 2H), 6.87 (d, 2H), 3.82 (s, 3H). 13C NMR (CD3OD) δ 166.8, 163.2, 162.7, 149.8, 130.8, 130.4, 128.2, 124.8, 116.3, 115.2, 55.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09085550B2 |
| Source dataset | uspto-grants-2015_07 |
| ORD ID | ord-c2428046e2234ad9a563aa4e456b7c49 |
| Source note | uspto-grants-2015_07 |