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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 458251Generated: October 30, 2026

2-hydroxy-N-[(E)-(4-hydroxy-3-methoxyphenyl)methylideneamino]-2-(4-methoxyphenyl)acetamide → hydroxy-(4-methoxy-phenyl)-acetic acid N'-(4-hydroxy-3-methoxy-benzyl)-hydrazide

https://huagongshe.com/reaction/458251

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-hydroxy-N-[(E)-(4-hydroxy-3-methoxyphenyl)methylideneamino]-2-(4-methoxyphenyl)acetamideHCID 136028530—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Producthydroxy-(4-methoxy-phenyl)-acetic acid N'-(4-hydroxy-3-methoxy-benzyl)-hydrazideHCID 58679590—

Reaction Steps

A solution of hydroxy-(4-methoxy-phenyl)-acetic acid [1-(4-hydroxy-3-methoxy-phenyl)-meth-(E)-ylidene]-hydrazide (21 g, 63 mmol) in 500 ml of ethanol is hydrogenated under atmospheric pressure with hydrogen and a mixture of 5% of palladium on charcoal (10.5 g) as catalyst. The reaction is stirred for 6 hours at room temperature. Subsequently, the mixture is filtered under argon and the solvent is evaporated to yield hydroxy-(4-methoxy-phenyl)-acetic acid N′-(4-hydroxy-3-methoxy-benzyl)-hydrazide as colourless tarr.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07189873B2
Source datasetuspto-grants-2007_03
ORD IDord-2005b31a35404372a2cba91eb3fe5172
Source noteuspto-grants-2007_03