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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274323Generated: November 3, 2026

Thiazolidinedione → 5-[4-(2-Hydroxy-2-phenylethoxy)benzylidene]-1,3-thiazolidine-2,4-dione

https://huagongshe.com/reaction/2274323

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiazolidinedioneHCID 5437—
ReactantPiperidineHCID 8082—
Reactant4-[(2S)-2-hydroxy-2-phenylethoxy]benzaldehydeHCID 86645071—
CatalystAcetic AcidHCID 176—
SolventEthanolHCID 702—
Product5-[4-(2-Hydroxy-2-phenylethoxy)benzylidene]-1,3-thiazolidine-2,4-dioneHCID 8664507086.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126959B2
Source datasetuspto-grants-2015_09
ORD IDord-6d5c42a2cffb4762ae8d824a09c74241
Source noteuspto-grants-2015_09