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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1587460Generated: November 4, 2026

3,4-Dihydroxybenzaldehyde → HCID 136331475, compound

https://huagongshe.com/reaction/1587460

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-DihydroxybenzaldehydeHCID 8768—
ReactantAcetamide, N-(aminocarbonyl)-2-cyano-HCID 74055—
CatalystPiperidineHCID 8082—
SolventEthanolHCID 702—
ProductHCID 136331475HCID 13633147560.7%

Reaction Steps

To 0.69 g (5 mmol) 3,4-dihydroxybenzaldehyde and 0.6 g (5.3 mmol) cyanoacetylurea in 40 ml ethanol was added 2 drops piperidine. The reaction mixture was refluxed for 2 hours, cooled, filtered and washed with cold ethanol to yield 0.75 g (60% yield) of a yellow-orange solid, m.p. 235° C. (decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05217999
Source datasetuspto-grants-1993_06
ORD IDord-58f0a97e644f4b60af08e49eec08a88e
Source noteuspto-grants-1993_06