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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1289153Generated: October 26, 2026

4-Thiazolidinone, 3-methyl-2-thioxo- → 5-[[4-[(4-Acetyl-3-hydroxy-2-propylphenyl)methoxy]phenyl]methylene]-3-methyl-2-thioxo-4-thiazolidinone

https://huagongshe.com/reaction/1289153

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Thiazolidinone, 3-methyl-2-thioxo-HCID 72900—
ReactantSodium AcetateHCID 517045—
Reactant4-[(4-Acetyl-3-hydroxy-2-propylphenyl)methoxy]benzaldehydeHCID 21191277—
SolventAcetic AcidHCID 176—
Product5-[[4-[(4-Acetyl-3-hydroxy-2-propylphenyl)methoxy]phenyl]methylene]-3-methyl-2-thioxo-4-thiazolidinoneHCID 86752507—

Reaction Conditions

Temperature100 °C

Reaction Steps

Under a nitrogen atmosphere in a three-neck round bottom flask 4-[(4-acetyl-3-hydroxy-2-propylphenyl)methoxy]benzaldehyde (90.0 mg, 0.29 mmol) was dissolved in acetic acid (1.5 ml) with stirring. To this solution was added sodium acetate (82.8 mg, 1.00 mmol) and N-methylrhodanine (42.5 mg, 0.29 mmol). The reaction mixture was then heated to 100° C. and maintained at this temperature for about two hours at which time the reaction mixture was raised to the reflux temperature and allowed to reflux for about 28 hours. The reaction progress was monitored by thin layer chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05747517
Source datasetuspto-grants-1998_05
ORD IDord-6ac4dd350dd24142ba206a5397064de6
Source noteuspto-grants-1998_05