HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4407Generated: October 28, 2026
HCID 13713937, compound → HCID 86741993, compound
https://huagongshe.com/reaction/4407
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 13713937 | HCID 13713937 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 86741993 | HCID 86741993 | 20% |
Reaction Steps
A solution of (Z)-5-{4-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]benzylidene}-2,4-thiazolidinedione (200 mg) in acetonitrile (750 ml), in a quartz tube under a stream of nitrogen, was irradiated by a 300 W high-pressure mercury lamp for 3 hours. The solvent was distilled off, and the resulting crystals were chromatographed on a column of silica gel (200 g). Elution with hexane-ethyl acetate (1:1, V/V) gave (E)-5-{4-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]benzylidene}-2,4-thiazolidinedione (40 mg, 20.0%). Recrystallization from dichloromethaneethanol yielded colorless needles, m.p. 216°-217° C. Elemental analysis for C22H18N2O4S; Calcd.: C, 65.01; H, 4.46; N, 6.89. Found: C, 64.69; H, 4.26; N, 7.11. The subsequent elution with hexane-ethyl acetate (1:1, V/v) allowed the recovery of (Z)-5-{4-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]benzylidene}-2,4-thiazolidinedione (138 mg, 69.0%).
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-760057bc35304f8ba2f1de1ab245109e |
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| Source note | uspto-grants-1988_02 |
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