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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6168Generated: October 25, 2026

Benzaldehyde → 5-Benzylidene-2,4-thiazolidinedione

https://huagongshe.com/reaction/6168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantThiazolidinedioneHCID 5437—
ReactantPiperidineHCID 8082—
SolventEthanolHCID 702—
Product5-Benzylidene-2,4-thiazolidinedioneHCID 19915490.4%

Reaction Steps

To a solution of 20 g (171 mmol) of 2,4-thiazolidinedione and 17.4 ml (171 mmol) of benzaldehyde 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 31.67 g of the desired compound (90.4% yield, pale yellow crystals).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05246948
Source datasetuspto-grants-1993_09
ORD IDord-f99fd64ecadc4d6fbfc0db3ce5607ef8
Source noteuspto-grants-1993_09