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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1873802Erstellt: 25. Oktober 2026

Thiazolidinedione → 5-[4-(2-Hydroxy-2-phenylethoxy)benzylidene]-1,3-thiazolidine-2,4-dione

https://huagongshe.com/reaction/1873802

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktThiazolidinedioneHCID 5437—
EduktPiperidineHCID 8082—
Edukt4-[(2S)-2-hydroxy-2-phenylethoxy]benzaldehydeHCID 86645071—
KatalysatorAcetic AcidHCID 176—
LösungsmittelEthanolHCID 702—
Produkt5-[4-(2-Hydroxy-2-phenylethoxy)benzylidene]-1,3-thiazolidine-2,4-dioneHCID 8664507086,3%

Reaktionsschritte

To a stirring solution of 4-[(2S)-2-hydroxy-2-phenylethoxy]benzaldehyde (2.63 g, 10.8 mmol) in absolute EtOH (75 ml) was added 2,4-thiazolidinedione (1.27 g, 10.8 mmol) and piperidine (0.54 mL, 5.4 mmol), and the resulting solution was heated to reflux. The reaction was refluxed overnight. The reaction mixture was allowed to cool to RT. No precipitate formed. The pH of reaction mixture was ca. 5. Acetic acid (20 drops) was added. The reaction was evaporated in vacuo. The material was adsorbed onto silica gel and chromatographed eluting with 30-40% EtOAc/hexanes. Fractions containing product were combined and evaporated in vacuo to give 3.18 g (86%) of the title compound as a light yellow solid. MS (ESI−) for C18H15NO4S m/z 340.1 (M−H)−.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08304441B2
Quelldatensatzuspto-grants-2012_11
ORD IDord-5bc7a5063f514d158530c26784107b4c
Quellennotizuspto-grants-2012_11