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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451816Generated: October 31, 2026

5-(Benzenesulfanyl)-thiazolidine-2,4-dione → 5-(Benzenesulfonyl)-thiazolidine-2,4-dione

https://huagongshe.com/reaction/1451816

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): δ8.07 (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=8.1 Hz, 2H, ArH), 5.44 (s, 1H CH); MS(EI): 225 (MI, 24%), 182 (18%), 153 (12%), 110 (100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05605918
Source datasetuspto-grants-1997_02
ORD IDord-33404c03a5154e36984dc89f8a075a6c
Source noteuspto-grants-1997_02