HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 517574Generated: October 30, 2026
Piperidine → (5Z)-5-(4-ethoxybenzylidene)-2-sulfanyl-1,3-thiazol-4(5H)-one
https://huagongshe.com/reaction/517574
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 4-Ethoxybenzaldehyde | HCID 24834 | — |
| Reactant | Rhodanine | HCID 1201546 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (5Z)-5-(4-ethoxybenzylidene)-2-sulfanyl-1,3-thiazol-4(5H)-one | HCID 5890514 | — |
Reaction Steps
4-Ethoxybenzaldehyde (2.78 mL, 20.00 mmol) and rhodanine 7 (3.75 g, 32.0 mmol) were dissolved in 80 mL of anhydrous ethanol at room temperature, and piperidine (0.60 mL, 6.0 mmol) was added to the reaction flask. The reaction mixture was stirred at 75° C. for 1 day and then allowed to cool down to room temperature until a yellow crystalline precipitate formed, and the solid was collected by filtration, washed with water and ethyl acetate, and dried to afford compound 8 in 80.0% (2.99 g) yield as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09115122B2 |
|---|
| Source dataset | uspto-grants-2015_08 |
|---|
| ORD ID | ord-a9587d0b35494316916f043c2df2be25 |
|---|
| Source note | uspto-grants-2015_08 |
|---|