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HRID 4386Erstellt: 26. Oktober 2026

Water → 5-[4-(2-Phenyl-4-oxazolylmethoxy)benzyl]-2,4-thiazolidinedione

https://huagongshe.com/reaction/4386

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium hydrideHCID 24758—
Edukt4-(Chloromethyl)-2-phenyl-1,3-oxazoleHCID 3551196—
Edukt5-(4-Hydroxybenzyl)thiazolidine-2,4-dioneHCID 10198397—
LösungsmittelDimethylformamideHCID 6228—
Produkt5-[4-(2-Phenyl-4-oxazolylmethoxy)benzyl]-2,4-thiazolidinedioneHCID 1371389356,8%

Reaktionsschritte

To a solution of 5-(4-hydroxybenzyl)-2,4-thiazolidinedione (9.4 g) in N,N-dimethylformamide (80 ml) was added 60% sodium hydride in oil (3.4 g), and the mixture was stirred for 30 minutes. Then, a solution of 4-chloromethyl-2-phenyloxazole (9.6 g) in N,N-dimethylformamide (20 ml) was added dropwise thereto at room temperature. After being stirred at 70° C. for 1 hour, the reaction solution was poured into water, and the aqueous mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with water, dried (MgSO4) and concentrated to give 5-[4-(2-phenyl-4-oxazolylmethoxy)benzyl]-2,4-thiazolidinedione (9.1 g, 47.4%). Recrystallization from ethanol yielded colorless needles. m.p. 188°-189° C. Elemental analysis for C20H16N2O4S; Calcd.: C, 63.15; H, 4.24; N, 7.36. Found: C, 63.19; H, 4.16; N, 7.23.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04725610
Quelldatensatzuspto-grants-1988_02
ORD IDord-35e63bd3939a469295f57ada34255d08
Quellennotizuspto-grants-1988_02