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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1281133Generated: November 1, 2026

Thiazolidinedione → HCID 72085102, compound

https://huagongshe.com/reaction/1281133

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiazolidinedioneHCID 5437—
ReactantPiperidineHCID 8082—
Reactant4-Bromothiophene-2-carbaldehydeHCID 87792—
SolventEthanolHCID 702—
ProductHCID 72085102HCID 7208510287.2%

Reaction Steps

To a mixture of 4-bromothiophene-2-carboxaldehyde (1.91 g, 10.0 mmol) and 2,4-thiazolidinedione (1.40 g, 12.0 mmol) in ethanol (30 mL) was added piperidine (1.0 mL, 10.0 mmol). The reaction mixture was heated at reflux for 3 h, then cooled on an ice-bath, and the precipitated products were collected by filtration. The cake was washed with 40% ethanol and dried to afford 5-(4-bromothiophen-2-ylmethylene)-2,4-thiazolidinedione (2.53 g, 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06452014B1
Source datasetuspto-grants-2002_09
ORD IDord-f1fa282738b840ddb40b25a4c4d9872a
Source noteuspto-grants-2002_09