HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1069120Generated: October 24, 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/en/reaction/1069120
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Thiazolidinone, 3-methyl-2-thioxo- | HCID 72900 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 4-[(4-Acetyl-3-hydroxy-2-propylphenyl)methoxy]benzaldehyde | HCID 21191277 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 5-[[4-[(4-Acetyl-3-hydroxy-2-propylphenyl)methoxy]phenyl]methylene]-3-methyl-2-thioxo-4-thiazolidinone | HCID 86752507 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06251928B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-03a655ea75a4460ca91808761dd55d17 |
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| Source note | uspto-grants-2001_06 |
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