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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(Benzenesulfanyl)-thiazolidine-2,4-dioneHCID 10489388—
ReactantHCID 10610046HCID 10610046—
ReactantPotassium hydroxy sulfiteHCID 23707502—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product5-(Benzenesulfonyl)-thiazolidine-2,4-dioneHCID 1053907473%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05574051
Source datasetuspto-grants-1996_11
ORD IDord-552f675f7974496cb3323a5e360d9cb8
Source noteuspto-grants-1996_11