戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 452782作成日:2026年10月26日

Antimony trichloride → 2-[3-[4-[(Fluoromethyl)thio]phenyl]-1-benzofuran-5-yl]-5-methyl-1,3,4-oxadiazole

https://huagongshe.com/reaction/452782

反応式

関与物質

役割名称HCID仕込み量
反応物Antimony trichlorideHCID 24814—
反応物(Bis(2-methoxyethyl)amino)sulfur trifluorideHCID 2734690—
反応物2-Methyl-5-[3-[4-(methylthio)phenyl]-1-benzofuran-5-yl]-1,3,4-oxadiazoleHCID 44481756—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl AcetateHCID 8857—
生成物2-[3-[4-[(Fluoromethyl)thio]phenyl]-1-benzofuran-5-yl]-5-methyl-1,3,4-oxadiazoleHCID 6866396230.4%

反応手順

To a solution of [bis(2-methoxyethyl)amino]sulfur trifluoride (1.38 mL, 7.50 mmol) in dichloromethane (10 mL) was added dropwise a solution of 2-methyl-5-[3-[4-(methylthio)phenyl]-1-benzofuran-5-yl]-1,3,4-oxadiazole (1.61 g, 5.00 mmol) in dichloromethane (15 mL) at room temperature. Antimony (III) chloride (0.0570 g, 0.250 mmol) was added to the solution, and the resulting mixture was stirred overnight at room temperature. The reaction mixture was diluted with ethyl acetate, washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/tetrahydrofuran=1/1) and recrystallized from hexane/ethyl acetate to give the title compound (517 mg, yield 30%) as pale-yellow crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08492378B2
出典データセットuspto-grants-2013_07
ORD IDord-f89e108746f840ab95f83b7d38c22bb8
出典メモuspto-grants-2013_07