HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795112Generated: October 31, 2026
Benzeneacetic acid, hydrazide → HCID 16075311, compound
https://huagongshe.com/reaction/1795112
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzeneacetic acid, hydrazide | HCID 70301 | — |
| Reactant | 2-(4-methylphenoxy)benzaldehyde | HCID 1474871 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 16075311 | HCID 16075311 | — |
Reaction Steps
To a solution of 2-(4-methylphenoxy)-benzaldehyde (500 mg, 2.36 mmol) in EtOH (10 mL) is added phenyl acetic hydrazide (336 mg, 2.36 mmol) and the reaction is heated to 80° C. for 1 h. While cooling a white precipitate forms, and this solid is isolated by filtration and washed with portions of EtOH and Et2O. This solid is dried under vacuum to provide N′-{(1E)-[2-(4-methylphenoxy)phenyl]methylene)}2-phenylacetohydrazide (432 mg, 22%). 1H-NMR (400 MHz, DMSO-d6) 11.70–11.55 (m, 1H), 8.51–8.33 (m, 1H), 8.00–7.92 (m, 1H), 7.42–7.19 (m, 9H), 6.91–6.85 (m, 3H), 3.98–3.43 (m, 2H), 2.29 (s, 3H). ESI+ for C22H20N2O2: m/z=345 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07026339B2 |
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| Source dataset | uspto-grants-2006_04 |
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| ORD ID | ord-8685dc68bb1142f9944892d4587bfeae |
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| Source note | uspto-grants-2006_04 |
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