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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1587457Generated: October 26, 2026

3,4-Dihydroxybenzaldehyde → 3,4-Dihydroxybenzylidenecyanoacethydrazide

https://huagongshe.com/reaction/1587457

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-DihydroxybenzaldehydeHCID 8768—
ReactantCyanoacetic acid hydrazideHCID 8820—
CatalystPiperidineHCID 8082—
SolventEthanolHCID 702—
Product3,4-DihydroxybenzylidenecyanoacethydrazideHCID 5372204850.2%

Reaction Steps

To 0.69 g (5 mmol) 3,4-dihydroxybenzaldehyde and 0.55 g (5.5 mmol) cyanoacethydrazide in 40 ml ethanol was added 2 drops piperidine. After 21/2 hours of reflux, the reaction mixture was cooled, filtered and washed with cold ethanol to give 0.55 g (50% yield) of product, an orange solid, m.p. 220° C. (decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05217999
Source datasetuspto-grants-1993_06
ORD IDord-ed1c041786bf46dfb55bb5c14b0a4e16
Source noteuspto-grants-1993_06