HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4393Generated: October 26, 2026
Water → 5-[4-(5-Methyl-2-phenyl-4-oxazolylmethoxy)benzylidene]-2,4-thiazolidinedione
https://huagongshe.com/reaction/4393
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-((4-Hydroxyphenyl)methylene)-2,4-thiazolidinedione | HCID 517822 | — |
| Reactant | 4-(Chloromethyl)-5-methyl-2-phenyl-1,3-oxazole | HCID 9794289 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-[4-(5-Methyl-2-phenyl-4-oxazolylmethoxy)benzylidene]-2,4-thiazolidinedione | HCID 54239028 | 41.6% |
Reaction Steps
60% sodium hydride in oil (0.24 g) was added to a solution of 5-(4-hydroxybenzylidene)-2,4-thiazolidinedione (0.664 g) in N,N-dimethylformamide (20 ml), and the mixture was stirred for 30 minutes. A solution of 4-chloromethyl-5-methyl-2-phenyloxazole (0.623 g) in N,N-dimethylformamide (10 ml) was added dropwise to the mixture under ice-cooling. After stirring at room temperature for 5 hours, the reaction solution was poured into water. The aqueous mixture was made acid with acetic acid and extracted with ethyl acetate. The ethyl acetate layer was washed with water, dried (MgSO4) and concentrated. The residue was chromatographed on a column of silica gel (50 g). From the fractions eluted with ethyl acetatehexane (1:2, V/V), there was obtained 5-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzylidene]-2,4-thiazolidinedione (0.49 g, 40.8%). Recrystallization from chloroform-methanol afforded colorless prisms, m.p. 225°-226° C. Elemental analysis for C21H16N2O4S, Calcd.: C, 64.27; H, 4.11; N, 7.14. Found: C, 64.49; H, 3.96; H, 6.86.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04725610 |
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| Source dataset | uspto-grants-1988_02 |
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| ORD ID | ord-59eb3a84c5114e449b61d0353ae198d1 |
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| Source note | uspto-grants-1988_02 |
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