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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 30642Erstellt: 24. Oktober 2026

4-Nitrobenzaldehyde → 5-(4-Nitrobenzylidene)-1,3-thiazolidine-2,4-dione

https://huagongshe.com/de/reaction/30642

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-NitrobenzaldehydeHCID 541—
EduktThiazolidinedioneHCID 5437—
EduktPiperidineHCID 8082—
LösungsmittelEthanolHCID 702—
Produkt5-(4-Nitrobenzylidene)-1,3-thiazolidine-2,4-dioneHCID 276826459,2%

Reaktionsschritte

A mixture of 4-nitrobenzaldehyde (15.1 g), 1,3-thiazolidine-2,4-dione (11.70 g), piperidine (1.70 g) and ethanol (300 mL) was heated under reflux for 24 hrs. The reaction mixture was concentrated. The obtained residue was washed with ethanol to give 5-(4-nitrobenzylidene)-1,3-thiazolidine-2,4-dione as yellow crystals (14.8 g, yield 59%). Recrystallization thereof from acetone-hexane gave pale-yellow prism crystals. melting point: 272-273° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07423159B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-02854ddf1583494d8386c11c20c29345
Quellennotizuspto-grants-2008_09