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HRID 6138作成日:2026年10月24日

N-3-Bromopropylphthalimide → 4-(3-Phthalimidopropyloxy)pyridine

https://huagongshe.com/ja/reaction/6138

反応式

関与物質

役割名称HCID仕込み量
反応物N-3-BromopropylphthalimideHCID 21611—
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-(3-Phthalimidopropyloxy)pyridineHCID 1907909016.4%

反応手順

To a solution of 4.76 g (50 mmol) of 4-hydroxypyridine and 14.75 g (55 mmol) of N-(3-bromopropyl)phthalimide in 80 ml of DMF was added 8.23 ml (55 mmol) of 1,8-diazabicyclo[5.4.0]-7-undecene. The mixture was stirred at room temperature for 6 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 the solvent was distilled off. The residue was purified by column chromatography (eluent: ethyl acetate) to obtain 2.32 g of the desired compound (yield: 16.4%, colorless crystals).

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-9416feec1e0e4637adb9bb2ca9dd4492
出典メモuspto-grants-1993_09