HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiazolidinedione → HCID 86616530, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiazolidinedione | HCID 5437 | — |
| Reactant | Piperidine, acetate | HCID 9793820 | — |
| Reactant | HCID 86616531 | HCID 86616531 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86616530 | HCID 86616530 | — |
Reaction Steps
To a solution of 3-methyl-4-(5-nitropyridin-2-yloxy)benzaldehyde (600 mg, 2.32 mmol) in toluene (35 mL) were added 2,4-thiazolidinedione (270 mg, 2.31 mmol) and piperidine acetate (135 mg, 0.93 mmol). The resulting solution was attached to a Dean Stark, and stirred under reflux for 1.5 hours. After being left to cool for 17 hours at room temperature, the precipitated yellow powder was filtered, to thereby yield 600 mg of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08236826B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-1bb1dc351693424d816c7fee097cfb5b |
| Source note | uspto-grants-2012_08 |