HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → 3-Amino-5-(4-phenoxybenzylidene)-2-thioxothiazolidin-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 4-Phenoxybenzaldehyde | HCID 66139 | — |
| Reactant | 3-Aminorhodanine | HCID 74033 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Amino-5-(4-phenoxybenzylidene)-2-thioxothiazolidin-4-one | HCID 501625 | 68.6% |
Reaction Steps
To a solution of 3-aminorhodanine (1.00 g) in ethanol (20 ml) were added 4-phenoxybenzaldehyde (1.47 g) and piperidine (57 mg), and the mixture was heated with reflux for 2 hr. The reaction mixture was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: chloroform) to give 3-amino-5-(4-phenoxybenzylidene)-2-thioxothiazolidin-4-one (1.52 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09056862B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-b798e8f2431342299a4913356416de04 |
| Source note | uspto-grants-2015_06 |