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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6169Generated: October 25, 2026

Thiazolidinedione → 5-(4-Chlorobenzylidene)-2,4-thiazolidinedione

https://huagongshe.com/reaction/6169

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiazolidinedioneHCID 5437—
Reactant4-ChlorobenzaldehydeHCID 7726—
ReactantPiperidineHCID 8082—
SolventEthanolHCID 702—
Product5-(4-Chlorobenzylidene)-2,4-thiazolidinedioneHCID 23307043.4%

Reaction Steps

To a solution of 20 g (171 mmol) of 2,4-thiazolidinedione and 17.4 ml (171 mmol) of 4-chlorobenzaldehyde in 350 ml of ethanol, 1.68 ml (17.1 mmol) of piperidine was added, and the mixture was heated under reflux for 5 hours. After cooling, the precipitated crystals were filtered and washed with cooled ethanol to give 17.75 g of the desired compound (43.4% yield, pale yellow crystals).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05246948
Source datasetuspto-grants-1993_09
ORD IDord-f955cb05073547f09e8e193f4ca25145
Source noteuspto-grants-1993_09