戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1048作成日:2026年10月23日

Dimethylformamide → 5-[2-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]ethyl]-1H-tetrazole

https://huagongshe.com/ja/reaction/1048

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Ammonium ChlorideHCID 25517—
反応物Sodium AzideHCID 33557—
反応物2-(2-Cyanoethyl)-6-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzofuranHCID 10155313—
溶媒WaterHCID 962—
生成物5-[2-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]ethyl]-1H-tetrazoleHCID 17841845178.1%

反応手順

A mixture of 2-(2-cyanoethyl)-6-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzofuran (1.20 g), sodium azide (1.09 g), ammonium chloride (0.90 g) and N,N-dimethylformamide (30 ml) was stirred at 130° to 140° C. for 16 hours. The reaction mixture was poured over water and extracted with ethyl acetate. After the ethyl acetate layer was washed with water and dried (MgSO4), the solvent was distilled off; the residue was subjected to silica gel column chromatography. From the fraction eluted with methanol-chloroform (5:95, v/v), 5-[2-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]ethyl ]-1H-tetrazole (1.05 g, 78%) was obtained, which was then recrystallized from dichloromethane-methanol to yield colorless prisms having a melting point of 177° to 178° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05723479
出典データセットuspto-grants-1998_03
ORD IDord-2e59b47848294fe195989e641f0b30fb
出典メモuspto-grants-1998_03