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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716056Generated: November 2, 2026

Thiazolidinedione → 3-Ethyl-2,4-thiazolidinedione

https://huagongshe.com/reaction/716056

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiazolidinedioneHCID 5437—
ReactantIodoethaneHCID 6340—
ReactantSodium hydrideHCID 24758—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product3-Ethyl-2,4-thiazolidinedioneHCID 516805180.7%

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187487B2
Source datasetuspto-grants-2015_11
ORD IDord-ea2852ca82b34478bb377f0959d75412
Source noteuspto-grants-2015_11