HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiazolidinedione → 5-[(3-Phenoxyphenyl)methylidene]-1,3-thiazolidine-2,4-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiazolidinedione | HCID 5437 | — |
| Reactant | 3-Phenoxybenzaldehyde | HCID 38284 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 5-[(3-Phenoxyphenyl)methylidene]-1,3-thiazolidine-2,4-dione | HCID 2854003 | — |
Reaction Conditions
| Temperature | 115 °C |
|---|
Reaction Steps
A solution of thiazolidine-2,4-dione (90%, 78 mg, 0.6 mmol) and ammonium acetate (92 mg, 1.2 mmol) in acetic acid (1 mL) was added to 3-phenoxybenzaldehyde (52 μL, 0.6 mmol) and the resulting mixture was shaken at 115° C. for 16 hours. After cooling, the mixture was concentrated in vacuo 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-ea3a5e1809b74e2e8c00deee8d274831 |
| Source note | uspto-grants-2011_02 |