HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1899877Generated: November 2, 2026
5-(Benzenesulfanyl)-thiazolidine-2,4-dione → 5-(Benzenesulfonyl)-thiazolidine-2,4-dione
https://huagongshe.com/reaction/1899877
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-(Benzenesulfanyl)-thiazolidine-2,4-dione | HCID 10489388 | — |
| Reactant | HCID 10610046 | HCID 10610046 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-(Benzenesulfonyl)-thiazolidine-2,4-dione | HCID 10539074 | 73% |
Reaction Steps
A solution of 5-(benzenesulfanyl)-thiazolidine-2,4-dione, [(III), Example 6, 10.0 g, 41.8 mmol] in methanol (105 mL) was added to a mechanically stirred suspension of oxone (51.4 g, 83.6 mmol) in water (210 mL) at 0° C. The suspension was immediately warmed to room temperature. After 3.5 h, the reaction was diluted with water (1.5 L) and the solid was filtered. The solid was washed with water and dried in vacuo to provide the title compound as a white solid (8.31 g, 73%): mp 130°-133° C.: NMR (CDCL3): δ 8.07 (s, 1H, NH), 7.98 (d, J=7.2 Hz, 2H, ArH) 7.78 (t, J=7.5 Hz, 1H, ArH), 7.67 (t, J=8.1Hz, 2H, ArH), 5.44 (s, 1H CH); MS(EI): 225 (MI, 24%), 182 (18%), 153 (12%), 110 (100%). By the procedure described in Example 15, the compounds of formula (V), Examples 16-18, were prepared from the appropriate 5-(arylsulfanyl)-thiazolidine-2,4-dione of formula (III).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05574051 |
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| Source dataset | uspto-grants-1996_11 |
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| ORD ID | ord-552f675f7974496cb3323a5e360d9cb8 |
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| Source note | uspto-grants-1996_11 |
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