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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360986Generated: October 26, 2026

Thiazolidinedione → 5-(3,4-Dibromobenzylidene)thiazolidine-2,4-dione

https://huagongshe.com/reaction/1360986

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiazolidinedioneHCID 5437—
ReactantPiperidineHCID 8082—
Reactant3,4-DibromobenzaldehydeHCID 622053—
SolventAcetic AcidHCID 176—
Product5-(3,4-Dibromobenzylidene)thiazolidine-2,4-dioneHCID 76545866—

Reaction Steps

A mixture of thiazolidine-2,4-dione (90%, 65 mg, 0.5 mmol), 3,4-dibromobenzaldehyde (132 mg, 0.5 mmol), and piperidine (247 μL, 2.5 mmol) was shaken in acetic acid (2 mL) at 110° C. for 16 hours. After cooling, the mixture was concentrated to dryness in vacuo. The resulting crude product was shaken with water, centrifuged, and the supernatant was discarded. Subsequently the residue was shaken with ethanol, centrifuged, the supernatant was discarded and the residue was further evaporated to dryness to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879893B2
Source datasetuspto-grants-2011_02
ORD IDord-1368f77cd1ce4057b5c4f1e0728b3996
Source noteuspto-grants-2011_02