HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoic Acid → 5-(2-(2-Chlorophenyl)benzylidene)thiazolidine-2,4-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoic Acid | HCID 243 | — |
| Reactant | Thiazolidinedione | HCID 5437 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 2'-Chloro-[1,1'-biphenyl]-2-carbaldehyde | HCID 1392375 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 5-(2-(2-Chlorophenyl)benzylidene)thiazolidine-2,4-dione | HCID 85108305 | — |
Reaction Steps
To a solution of 2-formyl-(2′-chloro-1,1′-biphenyl) (0.12 g, 0.55 mmol) and 2,4-thiazolidinedione (0.08 g, 0.65 mmol) in toluene (10 mL) were added piperidine (0.008 mL, 0.073 mMol) and benzoic acid (0.011 mg, 0.08 mmol), and the reaction was refluxed for 4 h with continuous removal of water. The solvent was then distilled off and the oily residue obtained was purified by chromatography on silica-gel using hexane: ethyl acetate (3:1) as the eluent to yield titled product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07348348B2 |
| Source dataset | uspto-grants-2008_03 |
| ORD ID | ord-32b984fe771643cc927f44d9582f6dee |
| Source note | uspto-grants-2008_03 |