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HRID 417993作成日:2026年10月24日

Oxalyl chloride → 3-Bromo-1-(4-fluorophenyl)piperazine 2,2-dimethylpropan-1-one

https://huagongshe.com/ja/reaction/417993

反応式

関与物質

役割名称HCID仕込み量
反応物Oxalyl chlorideHCID 65578—
反応物1-(4-Fluorophenyl)piperazineHCID 75260—
反応物DiisopropylethylamineHCID 81531—
反応物3-Bromo-2,2-dimethylpropanoic acidHCID 271932—
溶媒DichloromethaneHCID 6344—
生成物3-Bromo-1-(4-fluorophenyl)piperazine 2,2-dimethylpropan-1-oneHCID 8663578084%

反応手順

3-Bromo-2,2-dimethylpropionic acid (5.03 g, 27.8 mmol) was dissolved in DCM (60 mL). Oxalyl chloride (3.64 mL, 41.67 mmol) was added slowly over 10 minutes. The reaction mixture was stirred at room temperature for 18 hours and then concentrated in vacuo. The residue was dissolved in DCM (40 mL) and added to a solution of 4-fluorophenyl-piperazine (5.00 g, 27.8 mmol) and DIPEA (7.24 mL, 41.67 mmol) in DCM (30 mL) at 0° C. The reaction mixture was allowed to warm to room temperature over 1 hour and then stirred at room temperature for 16 hours. The reaction mixture was washed with 10% citric acid solution (2×100 mL), dried (MgSO4) and concentrated in vacuo to give 3-bromo-1-(4-fluorophenyl)piperazine-2,2-dimethylpropan-1-one (8.04 g, 84%) as a yellow solid which was used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08093248B2
出典データセットuspto-grants-2012_01
ORD IDord-03b004c3c8914e32964d2d6eb8016ce7
出典メモuspto-grants-2012_01