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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1525764Generated: November 5, 2026

4-Hydroxybenzoic acid hydrazide → 4-Hydroxy-N'-[(4-methoxyphenyl)methylidene]benzohydrazide

https://huagongshe.com/reaction/1525764

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Hydroxybenzoic acid hydrazideHCID 1742—
Reactant4-MethoxybenzaldehydeHCID 31244—
CatalystAcetic AcidHCID 176—
SolventEthanolHCID 702—
Product4-Hydroxy-N'-[(4-methoxyphenyl)methylidene]benzohydrazideHCID 31006894.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085550B2
Source datasetuspto-grants-2015_07
ORD IDord-c2428046e2234ad9a563aa4e456b7c49
Source noteuspto-grants-2015_07