Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 439554Generated: October 26, 2026

3-Chloro-4-hydroxy-5-methoxybenzaldehyde → 2-Cyano-3-(3-chloro-4-hydroxy-5-methoxyphenyl) propenanilide

https://huagongshe.com/reaction/439554

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-4-hydroxy-5-methoxybenzaldehydeHCID 29622—
ReactantAcetamide, 2-cyano-N-phenyl-HCID 69296—
CatalystPiperidineHCID 8082—
SolventEthanolHCID 702—
Product2-Cyano-3-(3-chloro-4-hydroxy-5-methoxyphenyl) propenanilideHCID 5418123874.1%

Reaction Steps

To a solution of 5-chlorovanillin (728 mg, 3.9 mmol) and cyanoacetanilide (625 mg, 3.9 mmol) in ethanol (20 ml) were added 3 drops of piperidine, and the resulting mixture was refluxed for 2 hours. After cooling to room temperature, the resulting solid was filtered and washed with ethanol: water (1: 1) to give the objective 2-cyano-3-(3-chloro-4-hydroxy-5-methoxyphenyl) propenanilide (950 mg, 74% in yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05514711
Source datasetuspto-grants-1996_05
ORD IDord-ab545d1684904c21bbf62432b3ba8d21
Source noteuspto-grants-1996_05