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HRID 6148作成日:2026年10月23日

1H-Isoindole-1,3(2H)-dione, 2-(2-bromoethyl)- → 4-(2-Phthalimidoethyloxy)pyridine

https://huagongshe.com/ja/reaction/6148

反応式

関与物質

役割名称HCID仕込み量
反応物1H-Isoindole-1,3(2H)-dione, 2-(2-bromoethyl)-HCID 11325—
反応物1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
反応物HCID 178418642HCID 178418642—
溶媒DimethylformamideHCID 6228—
生成物4-(2-Phthalimidoethyloxy)pyridineHCID 190792113.1%

反応手順

To a solution of 4.76 g (50 mmol) of 4-hydroxypyridine and 13.97 g (55 mmol) of N-(2-bromoethyl)phthalimide in 80 ml of DMF, 8.23 ml (55 mmol) of 1,8-diazabicyclo[5.4.0]-7-undecene was added. The mixture was stirred at room temperature for 32 hours. After the solvent was distilled off, the mixture was poured into water and extracted with ethyl acetate. The mixture was washed with water and dried over anhydrous magnesium sulfate, and then the solvent was distilled off. The residue was purified by column chromatography (eluent: ethyl acetate) to obtain 0.41 g of the desired compound (yield: 3.1%, colorless crystal).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05246948
出典データセットuspto-grants-1993_09
ORD IDord-73cf2bb5afde4483b79e29dae5dd822c
出典メモuspto-grants-1993_09