HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiazolidinedione → 5-(3,4-Dibromobenzylidene)thiazolidine-2,4-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiazolidinedione | HCID 5437 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 3,4-Dibromobenzaldehyde | HCID 622053 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 5-(3,4-Dibromobenzylidene)thiazolidine-2,4-dione | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07879893B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-1368f77cd1ce4057b5c4f1e0728b3996 |
| Source note | uspto-grants-2011_02 |