戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 635850作成日:2026年10月27日

Tetrahydrofuran → 1-(2,3-Dimethylimidazo[2,1-b][1,3]thiazol-5-yl)-3-phenylprop-2-en-1-ol

https://huagongshe.com/reaction/635850

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物Sodium borohydrideHCID 4311764—
反応物2,3-Dimethyl-(2-phenyl-E-ethenyl)imidazo[2,1-b]thiazol-5-yl methanoneHCID 21256502—
溶媒EthanolHCID 702—
生成物1-(2,3-Dimethylimidazo[2,1-b][1,3]thiazol-5-yl)-3-phenylprop-2-en-1-olHCID 467098—

反応手順

A solution of 2,3-Dimethyl-α-(2-phenyl-E-ethenyl)imidazo[2,1-b]thiazole-5-methanone (FIG. D-2) (0.34 g) in 1:1 ethanol:THF (40 mL) was treated with a solution of NaBH4 (0.35 g) in ethanol (5 mL). The solution was reacted for 2.5 hours, evaporated in vacuo, and the residue was diluted with water. The precipitated 2,3-Dimethyl-α-(2-phenylethenyl)imidazo[2,1-b]thiazole-5-methanol (FIG. D-5) was extracted into ethyl acetate, the extract was dried and evaporated to a viscous residue. The residue was triturated with ethyl acetate to yield 2,3-Dimethyl-α-(2-phenylethenyl)imidazo[2,1-b]thiazole-5-methanol (FIG. D-5), 0.28 g, m.p. 149-151° after crystallization from acetonitrile.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06191124B1
出典データセットuspto-grants-2001_02
ORD IDord-192b789b89b84680bdc5e6522e121c9e
出典メモuspto-grants-2001_02