HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716056Generated: November 2, 2026
Thiazolidinedione → 3-Ethyl-2,4-thiazolidinedione
https://huagongshe.com/reaction/716056
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thiazolidinedione | HCID 5437 | — |
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Ethyl-2,4-thiazolidinedione | HCID 5168051 | 80.7% |
Reaction Steps
To a 100 ml three necked round bottom flask, sodium hydride (60% in paraffin) (0.188 g, 0.00470 mole) was taken in DMF (2.0 ml). Thiazolidine-2,4-dione (0.5 g, 0.00427 mole) in DMF (3 ml) was slowly added at 0° C. over 15 min under nitrogen atmosphere. After addition was complete, the reaction mixture was stirred for 1 hr at 50° C. The reaction was then cooled to 0° C., followed by drop wise addition of ethyl iodide (0.41 ml, 0.00512 mole) at 0° C. The reaction mixture was warmed up to RT and stirred for 1 hr. After completion of the reaction, the reaction mixture was poured in water and aq. layer was extracted with ethyl acetate. Organic layers were combined and washed with brine solution, dried over Na2SO4, filtered and concentrated to afford crude product which was purified using column purification by eluting the compound with 5% ethyl acetate in hexanes to yield 0.5 g of 3-ethylthiazolidine-2,4-dione.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09187487B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-ea2852ca82b34478bb377f0959d75412 |
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| Source note | uspto-grants-2015_11 |
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