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HRID 4393作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium hydrideHCID 24758—
反応物5-((4-Hydroxyphenyl)methylene)-2,4-thiazolidinedioneHCID 517822—
反応物4-(Chloromethyl)-5-methyl-2-phenyl-1,3-oxazoleHCID 9794289—
溶媒Acetic AcidHCID 176—
溶媒DimethylformamideHCID 6228—
生成物5-[4-(5-Methyl-2-phenyl-4-oxazolylmethoxy)benzylidene]-2,4-thiazolidinedioneHCID 5423902841.6%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04725610
出典データセットuspto-grants-1988_02
ORD IDord-59eb3a84c5114e449b61d0353ae198d1
出典メモuspto-grants-1988_02