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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 4393Erstellt: 23. Oktober 2026

Water → 5-[4-(5-Methyl-2-phenyl-4-oxazolylmethoxy)benzylidene]-2,4-thiazolidinedione

https://huagongshe.com/de/reaction/4393

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium hydrideHCID 24758—
Edukt5-((4-Hydroxyphenyl)methylene)-2,4-thiazolidinedioneHCID 517822—
Edukt4-(Chloromethyl)-5-methyl-2-phenyl-1,3-oxazoleHCID 9794289—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelDimethylformamideHCID 6228—
Produkt5-[4-(5-Methyl-2-phenyl-4-oxazolylmethoxy)benzylidene]-2,4-thiazolidinedioneHCID 5423902841,6%

Reaktionsschritte

60% sodium hydride in oil (0.24 g) was added to a solution of 5-(4-hydroxybenzylidene)-2,4-thiazolidinedione (0.664 g) in N,N-dimethylformamide (20 ml), and the mixture was stirred for 30 minutes. A solution of 4-chloromethyl-5-methyl-2-phenyloxazole (0.623 g) in N,N-dimethylformamide (10 ml) was added dropwise to the mixture under ice-cooling. After stirring at room temperature for 5 hours, the reaction solution was poured into water. The aqueous mixture was made acid with acetic acid and extracted with ethyl acetate. The ethyl acetate layer was washed with water, dried (MgSO4) and concentrated. The residue was chromatographed on a column of silica gel (50 g). From the fractions eluted with ethyl acetatehexane (1:2, V/V), there was obtained 5-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzylidene]-2,4-thiazolidinedione (0.49 g, 40.8%). Recrystallization from chloroform-methanol afforded colorless prisms, m.p. 225°-226° C. Elemental analysis for C21H16N2O4S, Calcd.: C, 64.27; H, 4.11; N, 7.14. Found: C, 64.49; H, 3.96; H, 6.86.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04725610
Quelldatensatzuspto-grants-1988_02
ORD IDord-59eb3a84c5114e449b61d0353ae198d1
Quellennotizuspto-grants-1988_02