戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 4387作成日:2026年10月24日

Water → 5-{4-[2-(1-Methylcyclohexyl)-4-oxazolylmethoxy]benzyl}-2,4-thiazolidinedione

https://huagongshe.com/ja/reaction/4387

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-Hydroxybenzyl)thiazolidine-2,4-dioneHCID 10198397—
反応物4-Chloromethyl-2-(1-methylcyclohexyl)oxazoleHCID 20152406—
溶媒DimethylformamideHCID 6228—
生成物5-{4-[2-(1-Methylcyclohexyl)-4-oxazolylmethoxy]benzyl}-2,4-thiazolidinedioneHCID 13713903—

反応手順

60% sodium hydride in oil (1.32 g) was added to solution of 5-(4-hydroxybenzyl)-2,4-thiazolidinedione (3.35 g) in N,N-dimethylformamide (30 ml), and the mixture was stirred for 30 minutes. Then, solution of 4-chloromethyl-2-(1-methylcyclohexyl)oxazole (3.85 g) in N,N-dimethylformamide (5 ml) was added dropwise thereto at room temperature. After being stirred at 60° 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. The oily residue was chromatographed on a column of silica gel (70 g). Elution with hexaneethyl acetate (2:1, V/V) gave 5-{4-[2-(1-methylcyclohexyl)-4-oxazolylmethoxy]benzyl}-2,4-thiazolidinedione as an oily substance. A solution of sodium 2-ethylhexanoate in isopropanol (2N, 3 ml) was added to the oily substance, and treated with ether. The crystals which separated out were collected by filtration to give 5- {4-[2-(1-methylcyclohexyl)-4-oxazolylmethoxy]benzyl}-2,4-thiazolidinedione.sodium salt (2.3 g, 36.3%). Recrystallization from methanol afforded colorless plates. m.p. 285°-287° C. (decomp.) Elemental analysis for C21H23N2O4SNa, Calcd.: C, 59.70; H, 5.49; N, 6.63. Found: C, 59.76; H, 5.56; N, 6.82.

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-1600130bf31e4d3497fdf571ee839211
出典メモuspto-grants-1988_02