HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiazolidinedione → 5-(3,5-Di-tert-butyl-4-hydroxyphenyl)-methylene-2,4-thiazolidinedione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiazolidinedione | HCID 5437 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 3,5-Di-tert-butyl-4-hydroxybenzaldehyde | HCID 73219 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-(3,5-Di-tert-butyl-4-hydroxyphenyl)-methylene-2,4-thiazolidinedione | HCID 86747238 | 424.3% |
Reaction Steps
To a solution of 12.5 g (107 mmol) of 2,4-thiazolidinedione and 25.0 g (107 mmol) of 3,5-di-tert-butyl-4-hydroxybenzaldehyde in 300 ml of ethanol, 1.05 ml (10.7 mmol) of piperidine was added, and the mixture was heated under reflux for 5 hours. After cooling, the precipitated crystals were filtered and washed with cooled ethanol to give 15.23 g of the desired compound (42.8% yield, pale yellow crystals).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05246948 |
| Source dataset | uspto-grants-1993_09 |
| ORD ID | ord-06a787a9c29b4bc098767573585c59cc |
| Source note | uspto-grants-1993_09 |