Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1281110Generated: November 2, 2026

Hydrochloric Acid → 5-(4-Formylbenzylidene)-2,4-thiazolidinedione

https://huagongshe.com/reaction/1281110

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantThiazolidinedioneHCID 5437—
ReactantPiperidineHCID 8082—
Reactant4-(Diethoxymethyl)benzaldehydeHCID 595993—
SolventEthanolHCID 702—
Product5-(4-Formylbenzylidene)-2,4-thiazolidinedioneHCID 327277294%

Reaction Steps

To a mixture of terephthalaldehyde mono-(diethyl acetal) (3.96 mL, 20.0 mmol) and 2,4-thiazolidinedione (2.81 g, 24.0 mmol) in ethanol (40 mL) was added piperidine (2.0 mL, 20.0 mmol). The reaction mixture was heated to reflux for 4 h. After cooling on an ice-bath, hydrochloric acid (0.2 mol/L, 100 mL) was added and the precipitated products were collected by filtration. The cake was washed with water and dried. To a solution of this product (5.50 g) in tetrahydrofuran (180 mL) was added hydrochloric acid (1 mol/L, 18 mL) and the mixture was stirred at room temperature for 2 h. Water was added, and the precipitated products were collected by filtration to give 5-(4-formylbenzylidene)-2,4-thiazolidinedione (3.91 g, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06452014B1
Source datasetuspto-grants-2002_09
ORD IDord-00d6190d86bf45d49634465ea5675c6c
Source noteuspto-grants-2002_09