戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 885861作成日:2026年10月27日

Benzoyl chloride → 1-[4-(4-Benzoylpiperazin-1-yl)phenyl]ethanone

https://huagongshe.com/reaction/885861

反応式

関与物質

役割名称HCID仕込み量
反応物Benzoyl chlorideHCID 7412—
反応物Piperazin-4-ylacetophenoneHCID 97269—
溶媒DichloromethaneHCID 6344—
生成物1-[4-(4-Benzoylpiperazin-1-yl)phenyl]ethanoneHCID 124518890.9%

反応手順

Benzoyl chloride (0.341 ml, 2.94 mmol) was added dropwise to a stirred mixture of 1-(4-piperazin-1-yl-phenyl)-ethanone (500 mg, 2.45 mmol) and TEA (0.681 ml, 4.9 mmol) in DCM (25 ml). The resulting solution was stirred overnight at room temperature, then diluted with DCM and washed with water, with NaHCO3 (5% in H2O) and finally with citric acid (20% in H2O). The organic phase was dried over Na2SO4 and evaporated in vacuo. The resulting solid was triturated with di-isopropylether and filtered to give 687 mg of 1-[4-(4-benzoyl-piperazin-1-yl)-phenyl]-ethanone.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08242175B2
出典データセットuspto-grants-2012_08
ORD IDord-56f1b21b68304fcba970fb832ef0771c
出典メモuspto-grants-2012_08