HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404626Generated: October 26, 2026
Thiazolidinedione → 5-[4-(2-Hydroxy-2-phenylethoxy)benzylidene]-1,3-thiazolidine-2,4-dione
https://huagongshe.com/reaction/1404626
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thiazolidinedione | HCID 5437 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 4-[(2S)-2-hydroxy-2-phenylethoxy]benzaldehyde | HCID 86645071 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-[4-(2-Hydroxy-2-phenylethoxy)benzylidene]-1,3-thiazolidine-2,4-dione | HCID 86645070 | 86.3% |
Reaction Steps
To a stirring solution of 4-[(2S)-2-hydroxy-2-phenylethoxy]benzaldehyde (2.63 g, 10.8 mmol) in absolute EtOH (75 mL) was added 2,4-thiazolidinedione (1.27 g, 10.8 mmol) and piperidine (0.54 mL, 5.4 mmol), and the resulting solution was heated to reflux. The reaction was refluxed overnight. The reaction mixture was allowed to cool to RT. No precipitate formed. The pH of reaction mixture was ca. 5. Acetic acid (20 drops) was added, and the reaction was evaporated in vacuo. The material was adsorbed onto silica gel and chromatographed eluting with 30-40% EtOAc/hexanes. Fractions containing product were combined and evaporated in vacuo to give 3.18 g (86%) of the title compound as a light yellow solid. MS (ESI−) for C18H15NO4S m/z 340.1 (M−H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08912335B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-9fa9e83a51c945b883c57e894a5dcac0 |
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| Source note | uspto-grants-2014_12 |
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