Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873821Generated: October 31, 2026

Thiazolidinedione → HCID 25230336, compound

https://huagongshe.com/reaction/1873821

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiazolidinedioneHCID 5437—
ReactantPiperidineHCID 8082—
Reactant4-[2-Hydroxy-2-(2-methoxyphenyl)ethoxy]benzaldehydeHCID 86645077—
SolventEthanolHCID 702—
ProductHCID 25230336HCID 2523033680.2%

Reaction Steps

To a stirring solution of 4-[2-hydroxy-2-(2-methoxyphenyl)ethoxy]benzaldehyde (1.71 g, 6.28 mmol) in absolute EtOH (50 ml) was added 2,4-thiazolidinedione (0.81 g, 6.91 mmol) and piperidine (0.68 mL, 6.9 mmol), and the resulting solution was heated to reflux. The reaction was refluxed overnight and then evaporated in vacuo. The residue was dissolved in EtOAc and 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 on silica gel eluting with 20-40% EtOAc/DCM. Fractions containing product were combined and evaporated in vacuo to give 1.87 g (80%) of the title compound as a light yellow solid. MS (ESI−) for C19H17NO5S m/z 370.1 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304441B2
Source datasetuspto-grants-2012_11
ORD IDord-a37800e335bb4b43b196358810c5ca01
Source noteuspto-grants-2012_11