HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 562955Generated: October 30, 2026
Thiazolidinedione → HCID 86645080, compound
https://huagongshe.com/reaction/562955
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thiazolidinedione | HCID 5437 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 86645079 | HCID 86645079 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86645080 | HCID 86645080 | 89.4% |
Reaction Steps
To a stirring solution of 4-[2-(3-chlorophenyl)-2-hydroxyethoxy]benzaldehyde (1.08 g, 3.90 mmol) in absolute EtOH (50 ml) was added 2,4-thiazolidinedione (0.50 g, 4.29 mmol) and piperidine (0.42 mL, 4.3 mmol), and the resulting solution was heated to reflux and then stirred overnight at room temperature. The reaction mixture was evaporated in vacuo and the residue was dissolved in EtOAc. This solution was washed with aqueous HOAc (pH 5-6), brine, dried (Na2SO4), filtered and evaporated in vacuo. The residue was adsorbed onto silica gel and chromatographed eluting with 10-20% EtOAc/DCM. Fractions containing product were combined and evaporated in vacuo to give 1.31 g (89%) of the product as a light yellow solid. MS (ESI+) for C18H14ClNO4S m/z 375.0 (M+H)+. MS (ESI−) for C18H14ClNO4S m/z 374.1 (M−H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08067450B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-3743476c4616499b871c64ac7883606d |
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| Source note | uspto-grants-2011_11 |
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