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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274325Generated: October 26, 2026

Dimethyl Sulfoxide → 5-[4-(2-Oxo-2-phenylethoxy)benzyl]-1,3-thiazolidine-2,4-dione

https://huagongshe.com/reaction/2274325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantPhosphorus oxide (P4O10)HCID 14812—
Reactant5-[4-(2-Hydroxy-2-phenylethoxy)benzyl]-1,3-thiazolidine-2,4-dioneHCID 46911041—
SolventDichloromethaneHCID 6344—
Product5-[4-(2-Oxo-2-phenylethoxy)benzyl]-1,3-thiazolidine-2,4-dioneHCID 2520653740.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirring solution of 5-[4-(2-hydroxy-2-phenylethoxy)benzyl]-1,3-thiazolidine-2,4-dione (1.00 g, 2.91 mmol) in DCM (35 mL) was added DMSO (2 mL) and the solution was cooled to 0° C. Phosphorus pentoxide (0.83 g, 2.91 mmol) was added followed by triethylamine (1.8 mL, 13.1 mmol). The reaction was allowed to slowly warm to RT. After 2 hours, the reaction mixture was partitioned between DCM and water and the organic phase was washed with brine, dried (Na2SO4), filtered and evaporated in vacuo. The resulting yellow oil was chromatographed on silica gel eluting with 25-35% EtOAc/hexanes. Fractions containing product were combined and evaporated in vacuo to give 0.40 g (40%) of the title compound as a white solid. Trituration with ether afforded 245 mg of clean product. MS (ESI−) for C18H15NO4S m/z 340.1 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126959B2
Source datasetuspto-grants-2015_09
ORD IDord-d6c3773e0ef84026be9f925a92b619c8
Source noteuspto-grants-2015_09