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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357459Generated: November 4, 2026

Thiazolidinedione → HCID 86759063, compound

https://huagongshe.com/reaction/1357459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiazolidinedioneHCID 5437—
ReactantTriethylamineHCID 8471—
Reactant1,6-DibromohexaneHCID 12368—
SolventAcetonitrileHCID 6342—
ProductHCID 86759063HCID 8675906370%

Reaction Steps

36.6 g of 1,6-dibromohexane, 5.9 g of 2,4-thiazolidinedione and 7.1 g of triethylamine were added to 125 ml of acetonitrile and the mixture was heated with stirring under reflux for 8 hours. After cooling to room temperature, the solvent was evaporated under reduced pressure and the residue was poured into water. The mixture was extracted with methylene chloride and the methylene chloride layer was washed with saturated brine and dried over sodium sulfate. After the solvent was evaporated under reduced pressure, the residue was purified by silica gel column chromatography (hexane:ethyl acetate=5:1→4:1) to obtain 9.8 g of the title compound as pale yellow oil (yield: 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06593323B1
Source datasetuspto-grants-2003_07
ORD IDord-f78d7c3e2c7f40fcabbafea6af378558
Source noteuspto-grants-2003_07