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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1404628Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1404628

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfoxideHCID 679—
EduktTriethylamineHCID 8471—
EduktPhosphorus oxide (P4O10)HCID 14812—
Edukt5-[4-(2-Hydroxy-2-phenylethoxy)benzyl]-1,3-thiazolidine-2,4-dioneHCID 46911041—
LösungsmittelDichloromethaneHCID 6344—
Produkt5-[4-(2-Oxo-2-phenylethoxy)benzyl]-1,3-thiazolidine-2,4-dioneHCID 2520653740,3%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

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)−.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08912335B2
Quelldatensatzuspto-grants-2014_12
ORD IDord-43a7749da2de47c9870178956c239b0d
Quellennotizuspto-grants-2014_12