HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiazolidinedione → HCID 86759063, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiazolidinedione | HCID 5437 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,6-Dibromohexane | HCID 12368 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 86759063 | HCID 86759063 | 70% |
Reaction Steps
36.6 g of 1,6-dibromohexane, 5.9 g of 2,4-thiazolidinedione and 7.1 g of triethylamine were added to 125 ml of acetonitrile and the mixture was heated with stirring under reflux for 8 hours. After cooling to room temperature, the solvent was evaporated under reduced pressure and the residue was poured into water. The mixture was extracted with methylene chloride and the methylene chloride layer was washed with saturated brine and dried over sodium sulfate. After the solvent was evaporated under reduced pressure, the residue was purified by silica gel column chromatography (hexane:ethyl acetate=5:1→4:1) to obtain 9.8 g of the title compound as pale yellow oil (yield: 70%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06593323B1 |
| Source dataset | uspto-grants-2003_07 |
| ORD ID | ord-f78d7c3e2c7f40fcabbafea6af378558 |
| Source note | uspto-grants-2003_07 |